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nsv7027974

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18,060

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 261 SVs from 26 studies. See in: genome view    
    Submitted genomic81,413,015-81,431,074Question Mark
    Overlapping variant regions from other studies: 261 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):80,668,514-80,686,573Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7027974Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX81,413,01581,431,074
    nsv7027974RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX80,668,51480,686,573

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18767934inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18767934Submitted genomicNC_000023.11:g.814
    13015_81431074inv
    GRCh38 (hg38)NC_000023.11ChrX81,413,01581,431,074
    nssv18767934RemappedPerfectNC_000023.10:g.806
    68514_80686573inv
    GRCh37.p13First PassNC_000023.10ChrX80,668,51480,686,573

    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)
    nssv187679345e-061200000
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