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nsv7052621

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,507,544

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 7825 SVs from 87 studies. See in: genome view    
    Submitted genomic103,826,879-110,334,422Question Mark
    Overlapping variant regions from other studies: 7799 SVs from 87 studies. See in: genome view    
    Remapped(Score: Good):103,081,809-109,577,650Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7052621Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX103,826,879110,334,422
    nsv7052621RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX103,081,809109,577,650

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18765573inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18765573Submitted genomicNC_000023.11:g.103
    826879_110334422in
    v
    GRCh38 (hg38)NC_000023.11ChrX103,826,879110,334,422
    nssv18765573RemappedGoodNC_000023.10:g.103
    081809_109577650in
    v
    GRCh37.p13First PassNC_000023.10ChrX103,081,809109,577,650

    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)
    nssv187655735e-061200000
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