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nsv7092966

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,667,596

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3699 SVs from 74 studies. See in: genome view    
    Submitted genomic94,283,314-96,950,909Question Mark
    Overlapping variant regions from other studies: 3699 SVs from 74 studies. See in: genome view    
    Remapped(Score: Perfect):93,538,313-96,205,908Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7092966Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX94,283,31496,950,909
    nsv7092966RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX93,538,31396,205,908

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18657971duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18657971Submitted genomicNC_000023.11:g.942
    83314_96950909dup
    GRCh38 (hg38)NC_000023.11ChrX94,283,31496,950,909
    nssv18657971RemappedPerfectNC_000023.10:g.935
    38313_96205908dup
    GRCh37.p13First PassNC_000023.10ChrX93,538,31396,205,908

    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)
    nssv186579715e-061200000
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