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nsv7050206

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,806,024

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2532 SVs from 70 studies. See in: genome view    
    Submitted genomic130,371,007-132,177,030Question Mark
    Overlapping variant regions from other studies: 2538 SVs from 70 studies. See in: genome view    
    Remapped(Score: Good):129,504,981-131,311,058Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7050206Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX130,371,007132,177,030
    nsv7050206RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX129,504,981131,311,058

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18765409inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18765409Submitted genomicNC_000023.11:g.130
    371007_132177030in
    v
    GRCh38 (hg38)NC_000023.11ChrX130,371,007132,177,030
    nssv18765409RemappedGoodNC_000023.10:g.129
    504981_131311058in
    v
    GRCh37.p13First PassNC_000023.10ChrX129,504,981131,311,058

    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)
    nssv187654095e-061200000
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