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nsv6472163

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:425

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 88 SVs from 15 studies. See in: genome view    
    Submitted genomic117,252,179-117,252,603Question Mark
    Overlapping variant regions from other studies: 88 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):117,122,895-117,123,319Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6472163Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11117,252,179117,252,603
    nsv6472163RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11117,122,895117,123,319

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17987141deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17987141Submitted genomicNC_000011.10:g.117
    252179_117252603de
    l
    GRCh38 (hg38)NC_000011.10Chr11117,252,179117,252,603
    nssv17987141RemappedPerfectNC_000011.9:g.1171
    22895_117123319del
    GRCh37.p13First PassNC_000011.9Chr11117,122,895117,123,319

    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)
    nssv17987141<0.001134004
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