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nsv7066511

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:156,553

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 391 SVs from 62 studies. See in: genome view    
    Submitted genomic106,963,989-107,120,541Question Mark
    Overlapping variant regions from other studies: 391 SVs from 62 studies. See in: genome view    
    Remapped(Score: Perfect):109,726,270-109,882,822Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7066511Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9106,963,989107,120,541
    nsv7066511RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9109,726,270109,882,822

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18783182inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18783182Submitted genomicNC_000009.12:g.106
    963989_107120541in
    v
    GRCh38 (hg38)NC_000009.12Chr9106,963,989107,120,541
    nssv18783182RemappedPerfectNC_000009.11:g.109
    726270_109882822in
    v
    GRCh37.p13First PassNC_000009.11Chr9109,726,270109,882,822

    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)
    nssv187831824e-061276268
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