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nsv7052075

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:423,050

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 879 SVs from 54 studies. See in: genome view    
    Submitted genomic139,736,192-140,159,241Question Mark
    Overlapping variant regions from other studies: 879 SVs from 54 studies. See in: genome view    
    Remapped(Score: Good):138,818,351-139,241,403Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7052075Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX139,736,192140,159,241
    nsv7052075RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX138,818,351139,241,403

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18762915inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18762915Submitted genomicNC_000023.11:g.139
    736192_140159241in
    v
    GRCh38 (hg38)NC_000023.11ChrX139,736,192140,159,241
    nssv18762915RemappedGoodNC_000023.10:g.138
    818351_139241403in
    v
    GRCh37.p13First PassNC_000023.10ChrX138,818,351139,241,403

    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)
    nssv187629155e-061200000
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