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nsv7084407

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:702,916

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1002 SVs from 63 studies. See in: genome view    
    Submitted genomic137,757,922-138,460,837Question Mark
    Overlapping variant regions from other studies: 1002 SVs from 63 studies. See in: genome view    
    Remapped(Score: Perfect):136,840,081-137,542,995Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7084407Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX137,757,922138,460,837
    nsv7084407RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX136,840,081137,542,995

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18653708duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18653708Submitted genomicNC_000023.11:g.137
    757922_138460837du
    p
    GRCh38 (hg38)NC_000023.11ChrX137,757,922138,460,837
    nssv18653708RemappedPerfectNC_000023.10:g.136
    840081_137542995du
    p
    GRCh37.p13First PassNC_000023.10ChrX136,840,081137,542,995

    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)
    nssv186537085e-061200000
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