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nsv7041243

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:165,386

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 577 SVs from 45 studies. See in: genome view    
    Submitted genomic124,055,047-124,220,432Question Mark
    Overlapping variant regions from other studies: 577 SVs from 45 studies. See in: genome view    
    Remapped(Score: Perfect):123,188,897-123,354,282Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7041243Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX124,055,047124,220,432
    nsv7041243RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX123,188,897123,354,282

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18764710inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18764710Submitted genomicNC_000023.11:g.124
    055047_124220432in
    v
    GRCh38 (hg38)NC_000023.11ChrX124,055,047124,220,432
    nssv18764710RemappedPerfectNC_000023.10:g.123
    188897_123354282in
    v
    GRCh37.p13First PassNC_000023.10ChrX123,188,897123,354,282

    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)
    nssv187647105e-061200000
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