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nsv7044698

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,433,756

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4680 SVs from 80 studies. See in: genome view    
    Submitted genomic87,352,100-90,785,855Question Mark
    Overlapping variant regions from other studies: 4680 SVs from 80 studies. See in: genome view    
    Remapped(Score: Perfect):86,607,103-90,040,854Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7044698Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX87,352,10090,785,855
    nsv7044698RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX86,607,10390,040,854

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18765070inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18765070Submitted genomicNC_000023.11:g.873
    52100_90785855inv
    GRCh38 (hg38)NC_000023.11ChrX87,352,10090,785,855
    nssv18765070RemappedPerfectNC_000023.10:g.866
    07103_90040854inv
    GRCh37.p13First PassNC_000023.10ChrX86,607,10390,040,854

    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)
    nssv187650702.8e-056214286
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