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nsv6464659

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:384,726

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1117 SVs from 75 studies. See in: genome view    
    Submitted genomic37,834,858-38,219,583Question Mark
    Overlapping variant regions from other studies: 1117 SVs from 75 studies. See in: genome view    
    Remapped(Score: Perfect):37,856,408-38,241,133Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6464659Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1137,834,85838,219,583
    nsv6464659RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1137,856,40838,241,133

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18194695duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18194695Submitted genomicNC_000011.10:g.378
    34858_38219583dup
    GRCh38 (hg38)NC_000011.10Chr1137,834,85838,219,583
    nssv18194695RemappedPerfectNC_000011.9:g.3785
    6408_38241133dup
    GRCh37.p13First PassNC_000011.9Chr1137,856,40838,241,133

    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)
    nssv18194695<0.001139202
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