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nsv6649511

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,555

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 100 SVs from 20 studies. See in: genome view    
    Submitted genomic37,621,262-37,624,816Question Mark
    Overlapping variant regions from other studies: 100 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):38,086,934-38,090,488Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6649511Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr137,621,26237,624,816
    nsv6649511RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr138,086,93438,090,488

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18390593deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18390593Submitted genomicNC_000001.11:g.376
    21262_37624816del
    GRCh38 (hg38)NC_000001.11Chr137,621,26237,624,816
    nssv18390593RemappedPerfectNC_000001.10:g.380
    86934_38090488del
    GRCh37.p13First PassNC_000001.10Chr138,086,93438,090,488

    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)
    nssv183905934e-061275380
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