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nsv7066485

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:230,563

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 880 SVs from 75 studies. See in: genome view    
    Submitted genomic87,915,480-88,146,042Question Mark
    Overlapping variant regions from other studies: 880 SVs from 75 studies. See in: genome view    
    Remapped(Score: Perfect):90,530,395-90,760,957Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7066485Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr987,915,48088,146,042
    nsv7066485RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr990,530,39590,760,957

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18785612inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18785612Submitted genomicNC_000009.12:g.879
    15480_88146042inv
    GRCh38 (hg38)NC_000009.12Chr987,915,48088,146,042
    nssv18785612RemappedPerfectNC_000009.11:g.905
    30395_90760957inv
    GRCh37.p13First PassNC_000009.11Chr990,530,39590,760,957

    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)
    nssv187856127e-062274416
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