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nsv7057879

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,406

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 138 SVs from 20 studies. See in: genome view    
    Submitted genomic226,695,834-226,701,239Question Mark
    Overlapping variant regions from other studies: 141 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):226,883,535-226,888,940Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7057879Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1226,695,834226,701,239
    nsv7057879RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1226,883,535226,888,940

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18761226inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18761226Submitted genomicNC_000001.11:g.226
    695834_226701239in
    v
    GRCh38 (hg38)NC_000001.11Chr1226,695,834226,701,239
    nssv18761226RemappedPerfectNC_000001.10:g.226
    883535_226888940in
    v
    GRCh37.p13First PassNC_000001.10Chr1226,883,535226,888,940

    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)
    nssv187612262.9e-058274246
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