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nsv7073939

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:19,248

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 229 SVs from 42 studies. See in: genome view    
    Submitted genomic133,162,473-133,181,720Question Mark
    Overlapping variant regions from other studies: 229 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):134,174,717-134,193,964Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7073939Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8133,162,473133,181,720
    nsv7073939RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8134,174,717134,193,964

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18782697inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18782697Submitted genomicNC_000008.11:g.133
    162473_133181720in
    v
    GRCh38 (hg38)NC_000008.11Chr8133,162,473133,181,720
    nssv18782697RemappedPerfectNC_000008.10:g.134
    174717_134193964in
    v
    GRCh37.p13First PassNC_000008.10Chr8134,174,717134,193,964

    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)
    nssv18782697<0.001120274956
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