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nsv7088439

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:182

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 240 SVs from 26 studies. See in: genome view    
    Submitted genomic68,656,068-68,656,249Question Mark
    Overlapping variant regions from other studies: 240 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):67,875,910-67,876,091Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7088439Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX68,656,06868,656,249
    nsv7088439RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX67,875,91067,876,091

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18659053duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18659053Submitted genomicNC_000023.11:g.686
    56068_68656249dup
    GRCh38 (hg38)NC_000023.11ChrX68,656,06868,656,249
    nssv18659053RemappedPerfectNC_000023.10:g.678
    75910_67876091dup
    GRCh37.p13First PassNC_000023.10ChrX67,875,91067,876,091

    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)
    nssv186590539e-062222222
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