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nsv7086172

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:129,205

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 468 SVs from 37 studies. See in: genome view    
    Submitted genomic23,605,777-23,734,981Question Mark
    Overlapping variant regions from other studies: 469 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):23,623,894-23,753,098Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7086172Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX23,605,77723,734,981
    nsv7086172RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX23,623,89423,753,098

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18655184duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18655184Submitted genomicNC_000023.11:g.236
    05777_23734981dup
    GRCh38 (hg38)NC_000023.11ChrX23,605,77723,734,981
    nssv18655184RemappedPerfectNC_000023.10:g.236
    23894_23753098dup
    GRCh37.p13First PassNC_000023.10ChrX23,623,89423,753,098

    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)
    nssv186551844.2e-059214286
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