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nsv6865237

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:47,352

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 157 SVs from 46 studies. See in: genome view    
    Submitted genomic122,487,483-122,534,834Question Mark
    Overlapping variant regions from other studies: 157 SVs from 46 studies. See in: genome view    
    Remapped(Score: Perfect):125,249,762-125,297,113Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6865237Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9122,487,483122,534,834
    nsv6865237RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9125,249,762125,297,113

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18732934duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18732934Submitted genomicNC_000009.12:g.122
    487483_122534834du
    p
    GRCh38 (hg38)NC_000009.12Chr9122,487,483122,534,834
    nssv18732934RemappedPerfectNC_000009.11:g.125
    249762_125297113du
    p
    GRCh37.p13First PassNC_000009.11Chr9125,249,762125,297,113

    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)
    nssv187329344e-061275106
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