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nsv6871210

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:192

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 74 SVs from 18 studies. See in: genome view    
    Submitted genomic122,210,976-122,211,167Question Mark
    Overlapping variant regions from other studies: 74 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):124,973,255-124,973,446Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6871210Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9122,210,976122,211,167
    nsv6871210RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9124,973,255124,973,446

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18731531duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18731531Submitted genomicNC_000009.12:g.122
    210976_122211167du
    p
    GRCh38 (hg38)NC_000009.12Chr9122,210,976122,211,167
    nssv18731531RemappedPerfectNC_000009.11:g.124
    973255_124973446du
    p
    GRCh37.p13First PassNC_000009.11Chr9124,973,255124,973,446

    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)
    nssv187315316.7e-0515233758
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