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nsv6865963

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:34

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 100 SVs from 25 studies. See in: genome view    
    Submitted genomic112,418,709-112,418,742Question Mark
    Overlapping variant regions from other studies: 100 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):115,180,989-115,181,022Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6865963Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9112,418,709112,418,742
    nsv6865963RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9115,180,989115,181,022

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18562669deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18562669Submitted genomicNC_000009.12:g.112
    418709_112418742de
    l
    GRCh38 (hg38)NC_000009.12Chr9112,418,709112,418,742
    nssv18562669RemappedPerfectNC_000009.11:g.115
    180989_115181022de
    l
    GRCh37.p13First PassNC_000009.11Chr9115,180,989115,181,022

    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)
    nssv18562669<0.00140245674
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