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nsv7088448

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:348,940

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 621 SVs from 53 studies. See in: genome view    
    Submitted genomic68,724,869-69,073,808Question Mark
    Overlapping variant regions from other studies: 623 SVs from 53 studies. See in: genome view    
    Remapped(Score: Perfect):67,944,711-68,293,651Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7088448Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX68,724,86969,073,808
    nsv7088448RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX67,944,71168,293,651

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18659058duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18659058Submitted genomicNC_000023.11:g.687
    24869_69073808dup
    GRCh38 (hg38)NC_000023.11ChrX68,724,86969,073,808
    nssv18659058RemappedPerfectNC_000023.10:g.679
    44711_68293651dup
    GRCh37.p13First PassNC_000023.10ChrX67,944,71168,293,651

    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)
    nssv186590585e-061200000
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