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nsv6875984

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,452,961

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3442 SVs from 95 studies. See in: genome view    
    Submitted genomic12,949,792-14,402,752Question Mark
    Overlapping variant regions from other studies: 3448 SVs from 95 studies. See in: genome view    
    Remapped(Score: Perfect):12,949,791-14,402,751Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6875984Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr912,949,79214,402,752
    nsv6875984RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr912,949,79114,402,751

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18733399duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18733399Submitted genomicNC_000009.12:g.129
    49792_14402752dup
    GRCh38 (hg38)NC_000009.12Chr912,949,79214,402,752
    nssv18733399RemappedPerfectNC_000009.11:g.129
    49791_14402751dup
    GRCh37.p13First PassNC_000009.11Chr912,949,79114,402,751

    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)
    nssv187333994e-061273218
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