Feature suggestion : Regional Allele Frequency for Indels
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0
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227
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May 30, 2024
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The start position of SV and CNVs at the gnomAD browser might be the preceding position
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0
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142
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June 3, 2024
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Large difference in pLI from v2.1.1 to v4.1.0
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4
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274
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June 7, 2024
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Is my interpretation of LOEUF threshold correct?
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1
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246
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October 15, 2024
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GnomAD SVs v4 - discrepancy between hemizygote & male (XY) counts
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7
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222
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November 5, 2024
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gnomAD v4 genome and exome sample counts per genetic ancestry groups
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4
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205
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May 16, 2024
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Discrepant frequencies flag in VCF files?
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1
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157
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September 5, 2024
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Interpretation of Homozygous and Hemizygous Counts on gnomAD variants
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1
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258
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May 22, 2024
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gnomAD v4.1 liftover to hg19
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1
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263
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May 21, 2024
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Rare and common variants numbers
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1
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211
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September 6, 2024
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Number of variants in each vcf file
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2
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148
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July 23, 2024
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Constraint metric
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4
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119
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September 11, 2024
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Missing MT variant VCF file for gnomAD-v4 or v4.1
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2
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170
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May 24, 2024
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Topic Loading chunk 595 failed.(missing: https://gnomad.broadinstitute.org/js/595-fc9ff4040fdf0d877f0b.js)
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1
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141
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August 14, 2024
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Will there be a V4 non-cancer
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2
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125
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July 3, 2024
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Number of expected and observed pLoF variants for CYP8B1 looks unusual
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4
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100
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September 27, 2024
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About allele balance
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2
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140
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June 5, 2024
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Only need VCFs of healthy individuals
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1
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147
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July 29, 2024
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PhyloP Question- Different on UCSC browser
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1
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146
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July 11, 2024
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gnomAD Copy number variants bed files
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3
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86
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September 3, 2024
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Number of observed variants vs hail query (v4.1.0)
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3
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92
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September 7, 2024
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Genotype quality for assessing CNV in gnomAD SV v4?
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1
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167
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July 22, 2024
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Ancestry inference params in v4
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1
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148
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June 5, 2024
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dbSNP156 vs gnomAD WGS
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1
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101
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September 17, 2024
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Variant Co-Occurrence table headings
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4
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72
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February 3, 2025
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Discrepancy between gnomAD and UK Biobank
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2
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81
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November 5, 2024
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MNV in gnomad 4.1
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1
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126
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July 2, 2024
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SV end position not equal to the start + sv length
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1
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125
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June 20, 2024
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Can I find HGVS Consequence of variant ID in gnomad.vcf.bgz?
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3
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73
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January 10, 2025
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Does gnomAD have access to the clinical status of individuals included in their data?
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1
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97
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September 5, 2024
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List of variants databases
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1
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121
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July 2, 2024
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gnomAD v4.1 not working?
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2
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71
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July 19, 2024
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Difference between V2 and V4
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1
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90
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August 27, 2024
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SV genotype quality threshold
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1
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134
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June 20, 2024
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V4 vs v4-nonUKB CFTR F508del
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1
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91
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October 4, 2024
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Cannot complete (or even view) user survey
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2
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83
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June 20, 2024
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Differences for LC_pLoF flags between v4.1.0 and v2.1.1
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1
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93
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October 28, 2024
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pLoF Metrics by Gene TSV columns
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3
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60
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December 11, 2024
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PhyloP indel scores
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1
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73
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February 13, 2025
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XX and XY sample numbers for v4 exomes and genomes
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1
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114
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June 28, 2024
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V4.1 Structural Variants BED files
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1
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69
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July 29, 2024
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What is the estimated relative distribution of gnomAD ancestry groups in the global population?
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1
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88
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June 27, 2024
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Rounding the frequencies in the browser
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3
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54
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September 10, 2024
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gnomAD v.4.1 API?
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1
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63
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January 24, 2025
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Ancestry RF classifer code and scripts
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6
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44
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May 9, 2025
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File containing binned methylation level of SNVs
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3
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51
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September 6, 2024
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Congenital Heart Defects - Screened out?
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1
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70
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June 27, 2024
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Assistance with Querying Non-Synonymous Variants for Specific Transcript ID
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2
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45
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August 9, 2024
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Geographical place of origin of samples
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1
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51
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September 11, 2024
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Access to Download
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1
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50
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October 16, 2024
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