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nsv6915703

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 67 SVs from 24 studies. See in: genome view    
    Submitted genomic8,464,701-8,468,500Question Mark
    Overlapping variant regions from other studies: 67 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):8,486,248-8,490,047Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6915703Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr118,464,7018,468,500
    nsv6915703RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr118,486,2488,490,047

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18575394duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18575394Submitted genomicNC_000011.10:g.846
    4701_8468500dup
    GRCh38 (hg38)NC_000011.10Chr118,464,7018,468,500
    nssv18575394RemappedPerfectNC_000011.9:g.8486
    248_8490047dup
    GRCh37.p13First PassNC_000011.9Chr118,486,2488,490,047

    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)
    nssv185753947e-062273574
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