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nsv7042376

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:64,247

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 484 SVs from 51 studies. See in: genome view    
    Submitted genomic123,759,737-123,823,983Question Mark
    Overlapping variant regions from other studies: 484 SVs from 51 studies. See in: genome view    
    Remapped(Score: Perfect):122,893,587-122,957,833Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7042376Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX123,759,737123,823,983
    nsv7042376RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX122,893,587122,957,833

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18764704inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18764704Submitted genomicNC_000023.11:g.123
    759737_123823983in
    v
    GRCh38 (hg38)NC_000023.11ChrX123,759,737123,823,983
    nssv18764704RemappedPerfectNC_000023.10:g.122
    893587_122957833in
    v
    GRCh37.p13First PassNC_000023.10ChrX122,893,587122,957,833

    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)
    nssv187647045e-061200000
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