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nsv7084046

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:472,842

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 801 SVs from 55 studies. See in: genome view    
    Submitted genomic133,802,954-134,275,795Question Mark
    Overlapping variant regions from other studies: 802 SVs from 55 studies. See in: genome view    
    Remapped(Score: Good):132,936,981-133,409,825Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7084046Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX133,802,954134,275,795
    nsv7084046RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX132,936,981133,409,825

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18655394duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18655394Submitted genomicNC_000023.11:g.133
    802954_134275795du
    p
    GRCh38 (hg38)NC_000023.11ChrX133,802,954134,275,795
    nssv18655394RemappedGoodNC_000023.10:g.132
    936981_133409825du
    p
    GRCh37.p13First PassNC_000023.10ChrX132,936,981133,409,825

    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)
    nssv186553941.4e-053214286
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