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nsv7067997

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,206,588

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 14861 SVs from 129 studies. See in: genome view    
    Submitted genomic8,181,479-12,388,066Question Mark
    Overlapping variant regions from other studies: 14861 SVs from 129 studies. See in: genome view    
    Remapped(Score: Perfect):8,039,001-12,245,575Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7067997Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr88,181,47912,388,066
    nsv7067997RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr88,039,00112,245,575

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18785390inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18785390Submitted genomicNC_000008.11:g.818
    1479_12388066inv
    GRCh38 (hg38)NC_000008.11Chr88,181,47912,388,066
    nssv18785390RemappedPerfectNC_000008.10:g.803
    9001_12245575inv
    GRCh37.p13First PassNC_000008.10Chr88,039,00112,245,575

    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)
    nssv187853904e-061276268
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