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nsv7092471

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:399

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 228 SVs from 19 studies. See in: genome view    
    Submitted genomic74,032,491-74,032,889Question Mark
    Overlapping variant regions from other studies: 228 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):73,252,326-73,252,724Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7092471Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX74,032,49174,032,889
    nsv7092471RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX73,252,32673,252,724

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18660679duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18660679Submitted genomicNC_000023.11:g.740
    32491_74032889dup
    GRCh38 (hg38)NC_000023.11ChrX74,032,49174,032,889
    nssv18660679RemappedPerfectNC_000023.10:g.732
    52326_73252724dup
    GRCh37.p13First PassNC_000023.10ChrX73,252,32673,252,724

    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)
    nssv186606791.4e-053214286
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