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nsv7092142

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:652,238

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 847 SVs from 58 studies. See in: genome view    
    Submitted genomic63,819,498-64,471,735Question Mark
    Overlapping variant regions from other studies: 803 SVs from 57 studies. See in: genome view    
    Remapped(Score: Pass):63,086,231-63,691,615Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7092142Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX63,819,49864,471,735
    nsv7092142RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX63,086,23163,691,615

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18656462duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18656462Submitted genomicNC_000023.11:g.638
    19498_64471735dup
    GRCh38 (hg38)NC_000023.11ChrX63,819,49864,471,735
    nssv18656462RemappedPassNC_000023.10:g.630
    86231_63691615dup
    GRCh37.p13First PassNC_000023.10ChrX63,086,23163,691,615

    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)
    nssv186564625e-061200000
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