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nsv7050440

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:626,422

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1255 SVs from 78 studies. See in: genome view    
    Submitted genomic141,157,879-141,784,300Question Mark
    Overlapping variant regions from other studies: 1234 SVs from 76 studies. See in: genome view    
    Remapped(Score: Good):140,252,077-140,872,086Question Mark
    Overlapping variant regions from other studies: 444 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):253,682-880,103Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7050440Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX141,157,879141,784,300
    nsv7050440RemappedGoodGRCh37.p13Primary AssemblySecond PassNC_000023.10ChrX140,252,077140,872,086
    nsv7050440RemappedPerfectGRCh37.p13PATCHESFirst PassNW_004070888.1ChrX|NW_00
    4070888.1
    253,682880,103

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18762952inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18762952Submitted genomicNC_000023.11:g.141
    157879_141784300in
    v
    GRCh38 (hg38)NC_000023.11ChrX141,157,879141,784,300
    nssv18762952RemappedPerfectNW_004070888.1:g.2
    53682_880103inv
    GRCh37.p13First PassNW_004070888.1ChrX|NW_00
    4070888.1
    253,682880,103
    nssv18762952RemappedGoodNC_000023.10:g.140
    252077_140872086in
    v
    GRCh37.p13Second PassNC_000023.10ChrX140,252,077140,872,086

    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)
    nssv187629525e-061200000
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