nsv7053106

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,636,038

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3376 SVs from 75 studies. See in: genome view    
    Submitted genomic118,857,141-120,493,178Question Mark
    Overlapping variant regions from other studies: 3372 SVs from 75 studies. See in: genome view    
    Remapped(Score: Good):117,991,104-119,627,033Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7053106Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX118,857,141120,493,178
    nsv7053106RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX117,991,104119,627,033

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18764627inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18764627Submitted genomicNC_000023.11:g.118
    857141_120493178in
    v
    GRCh38 (hg38)NC_000023.11ChrX118,857,141120,493,178
    nssv18764627RemappedGoodNC_000023.10:g.117
    991104_119627033in
    v
    GRCh37.p13First PassNC_000023.10ChrX117,991,104119,627,033

    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)
    nssv18764627<0.00136216867
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