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nsv7080536

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:72,942

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 366 SVs from 31 studies. See in: genome view    
    Submitted genomic23,235,250-23,308,191Question Mark
    Overlapping variant regions from other studies: 367 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):23,253,367-23,326,308Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7080536Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX23,235,25023,308,191
    nsv7080536RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX23,253,36723,326,308

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18655168duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18655168Submitted genomicNC_000023.11:g.232
    35250_23308191dup
    GRCh38 (hg38)NC_000023.11ChrX23,235,25023,308,191
    nssv18655168RemappedPerfectNC_000023.10:g.232
    53367_23326308dup
    GRCh37.p13First PassNC_000023.10ChrX23,253,36723,326,308

    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)
    nssv186551681.4e-053214286
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