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nsv6320974

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:30,816

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 250 SVs from 38 studies. See in: genome view    
    Submitted genomic47,407,616-47,438,431Question Mark
    Overlapping variant regions from other studies: 250 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):47,873,288-47,904,103Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6320974Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr147,407,61647,438,431
    nsv6320974RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr147,873,28847,904,103

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18201397duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18201397Submitted genomicNC_000001.11:g.474
    07616_47438431dup
    GRCh38 (hg38)NC_000001.11Chr147,407,61647,438,431
    nssv18201397RemappedPerfectNC_000001.10:g.478
    73288_47904103dup
    GRCh37.p13First PassNC_000001.10Chr147,873,28847,904,103

    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)
    nssv18201397<0.001139276
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