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nsv7034979

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,599,820

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3294 SVs from 93 studies. See in: genome view    
    Submitted genomic46,796,509-48,396,328Question Mark
    Overlapping variant regions from other studies: 3302 SVs from 93 studies. See in: genome view    
    Remapped(Score: Perfect):46,655,944-48,255,770Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7034979Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX46,796,50948,396,328
    nsv7034979RemappedPerfectGRCh37.p13Primary AssemblySecond PassNC_000023.10ChrX46,655,94448,255,770

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18766920inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18766920Submitted genomicNC_000023.11:g.467
    96509_48396328inv
    GRCh38 (hg38)NC_000023.11ChrX46,796,50948,396,328
    nssv18766920RemappedPerfectNC_000023.10:g.466
    55944_48255770inv
    GRCh37.p13Second PassNC_000023.10ChrX46,655,94448,255,770

    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)
    nssv187669205e-061200000
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