SNV and INDEL varaints from 125,748 exomes in the gnomAD dataset version 2.1.1 in bcf format. These variants were lifted over from gnomAD v2.1.1 GRCh37 to GRCh38 by the gnomAD group. The file constains all subsets of non-neuro, non-cancer, controls-only, and non-TOPMed samples. Remapped from Ensembl GRCh38 to UCSC hg38
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Summary
SNV and INDEL varaints from 125,748 exomes in the gnomAD dataset version 2.1.1 in bcf format. These variants were lifted over from gnomAD v2.1.1 GRCh37 to GRCh38 by the gnomAD group. The file constains all subsets of non-neuro, non-cancer, controls-only, and non-TOPMed samples. Remapped from Ensembl GRCh38 to UCSC hg38
Last Updated
Oct 2, 2020 at 15:53
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