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nsv7040336

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:106,340

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 796 SVs from 80 studies. See in: genome view    
    Submitted genomic143,861,334-143,967,673Question Mark
    Overlapping variant regions from other studies: 796 SVs from 80 studies. See in: genome view    
    Remapped(Score: Perfect):144,782,487-144,888,826Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7040336Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4143,861,334143,967,673
    nsv7040336RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4144,782,487144,888,826

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18772610inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18772610Submitted genomicNC_000004.12:g.143
    861334_143967673in
    v
    GRCh38 (hg38)NC_000004.12Chr4143,861,334143,967,673
    nssv18772610RemappedPerfectNC_000004.11:g.144
    782487_144888826in
    v
    GRCh37.p13First PassNC_000004.11Chr4144,782,487144,888,826

    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)
    nssv187726101.1e-053274640
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