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nsv7043190

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,362,102

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 18220 SVs from 123 studies. See in: genome view    
    Submitted genomic123,472,699-130,834,800Question Mark
    Overlapping variant regions from other studies: 17195 SVs from 123 studies. See in: genome view    
    Remapped(Score: Pass):123,112,753-129,984,423Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7043190Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7123,472,699130,834,800
    nsv7043190RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7123,112,753129,984,423

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18778918inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18778918Submitted genomicNC_000007.14:g.123
    472699_130834800in
    v
    GRCh38 (hg38)NC_000007.14Chr7123,472,699130,834,800
    nssv18778918RemappedPassNC_000007.13:g.123
    112753_129984423in
    v
    GRCh37.p13First PassNC_000007.13Chr7123,112,753129,984,423

    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)
    nssv187789184e-061276268
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