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nsv7067587

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:57,434

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 368 SVs from 56 studies. See in: genome view    
    Submitted genomic135,458,655-135,516,088Question Mark
    Overlapping variant regions from other studies: 368 SVs from 56 studies. See in: genome view    
    Remapped(Score: Perfect):138,350,501-138,407,934Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7067587Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9135,458,655135,516,088
    nsv7067587RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9138,350,501138,407,934

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18785650inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18785650Submitted genomicNC_000009.12:g.135
    458655_135516088in
    v
    GRCh38 (hg38)NC_000009.12Chr9135,458,655135,516,088
    nssv18785650RemappedPerfectNC_000009.11:g.138
    350501_138407934in
    v
    GRCh37.p13First PassNC_000009.11Chr9138,350,501138,407,934

    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)
    nssv187856504e-061276268
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