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nsv6974191

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12,359

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 195 SVs from 37 studies. See in: genome view    
    Submitted genomic3,709,936-3,722,294Question Mark
    Overlapping variant regions from other studies: 195 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):3,759,937-3,772,295Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6974191Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr163,709,9363,722,294
    nsv6974191RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr163,759,9373,772,295

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18401951deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18401951Submitted genomicNC_000016.10:g.370
    9936_3722294del
    GRCh38 (hg38)NC_000016.10Chr163,709,9363,722,294
    nssv18401951RemappedPerfectNC_000016.9:g.3759
    937_3772295del
    GRCh37.p13First PassNC_000016.9Chr163,759,9373,772,295

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv184019511.8e-055276232
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