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nsv7047243

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,013,919

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 6209 SVs from 119 studies. See in: genome view    
    Submitted genomic140,412,248-142,426,166Question Mark
    Overlapping variant regions from other studies: 5778 SVs from 118 studies. See in: genome view    
    Remapped(Score: Good):140,112,048-142,048,195Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7047243Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7140,412,248142,426,166
    nsv7047243RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7140,112,048142,048,195

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18781334inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18781334Submitted genomicNC_000007.14:g.140
    412248_142426166in
    v
    GRCh38 (hg38)NC_000007.14Chr7140,412,248142,426,166
    nssv18781334RemappedGoodNC_000007.13:g.140
    112048_142048195in
    v
    GRCh37.p13First PassNC_000007.13Chr7140,112,048142,048,195

    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)
    nssv18781334<0.00198271940
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