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nsv6459961

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:379,753

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1213 SVs from 85 studies. See in: genome view    
    Submitted genomic37,727,568-38,107,320Question Mark
    Overlapping variant regions from other studies: 1213 SVs from 85 studies. See in: genome view    
    Remapped(Score: Perfect):37,749,118-38,128,870Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6459961Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1137,727,56838,107,320
    nsv6459961RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1137,749,11838,128,870

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17990523deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17990523Submitted genomicNC_000011.10:g.377
    27568_38107320del
    GRCh38 (hg38)NC_000011.10Chr1137,727,56838,107,320
    nssv17990523RemappedPerfectNC_000011.9:g.3774
    9118_38128870del
    GRCh37.p13First PassNC_000011.9Chr1137,749,11838,128,870

    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)
    nssv17990523<0.001138990
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