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nsv7083208

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:264,825

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 896 SVs from 57 studies. See in: genome view    
    Submitted genomic119,748,932-120,013,756Question Mark
    Overlapping variant regions from other studies: 771 SVs from 54 studies. See in: genome view    
    Remapped(Score: Pass):118,882,895-119,081,533Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7083208Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX119,748,932120,013,756
    nsv7083208RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX118,882,895119,081,533

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18654263duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18654263Submitted genomicNC_000023.11:g.119
    748932_120013756du
    p
    GRCh38 (hg38)NC_000023.11ChrX119,748,932120,013,756
    nssv18654263RemappedPassNC_000023.10:g.118
    882895_119081533du
    p
    GRCh37.p13First PassNC_000023.10ChrX118,882,895119,081,533

    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)
    nssv186542635e-061200000
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