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nsv7066047

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:699,330

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1576 SVs from 75 studies. See in: genome view    
    Submitted genomic122,371,847-123,071,176Question Mark
    Overlapping variant regions from other studies: 1576 SVs from 75 studies. See in: genome view    
    Remapped(Score: Perfect):125,134,126-125,833,455Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7066047Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9122,371,847123,071,176
    nsv7066047RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9125,134,126125,833,455

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18784326inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18784326Submitted genomicNC_000009.12:g.122
    371847_123071176in
    v
    GRCh38 (hg38)NC_000009.12Chr9122,371,847123,071,176
    nssv18784326RemappedPerfectNC_000009.11:g.125
    134126_125833455in
    v
    GRCh37.p13First PassNC_000009.11Chr9125,134,126125,833,455

    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)
    nssv187843264e-061276266
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