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nsv6976536

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:267,445

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 704 SVs from 59 studies. See in: genome view    
    Submitted genomic93,740,828-94,008,272Question Mark
    Overlapping variant regions from other studies: 704 SVs from 59 studies. See in: genome view    
    Remapped(Score: Perfect):94,284,057-94,551,501Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6976536Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1593,740,82894,008,272
    nsv6976536RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1594,284,05794,551,501

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18617563duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18617563Submitted genomicNC_000015.10:g.937
    40828_94008272dup
    GRCh38 (hg38)NC_000015.10Chr1593,740,82894,008,272
    nssv18617563RemappedPerfectNC_000015.9:g.9428
    4057_94551501dup
    GRCh37.p13First PassNC_000015.9Chr1594,284,05794,551,501

    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)
    nssv186175637e-062275686
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