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nsv7083703

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:429,575

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 836 SVs from 58 studies. See in: genome view    
    Submitted genomic130,379,069-130,808,643Question Mark
    Overlapping variant regions from other studies: 836 SVs from 58 studies. See in: genome view    
    Remapped(Score: Perfect):129,513,043-129,942,617Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7083703Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX130,379,069130,808,643
    nsv7083703RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX129,513,043129,942,617

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18652980duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18652980Submitted genomicNC_000023.11:g.130
    379069_130808643du
    p
    GRCh38 (hg38)NC_000023.11ChrX130,379,069130,808,643
    nssv18652980RemappedPerfectNC_000023.10:g.129
    513043_129942617du
    p
    GRCh37.p13First PassNC_000023.10ChrX129,513,043129,942,617

    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)
    nssv186529805e-061200000
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