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nsv7074600

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,543

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 173 SVs from 30 studies. See in: genome view    
    Submitted genomic35,327,318-35,329,860Question Mark
    Overlapping variant regions from other studies: 180 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):35,327,315-35,329,857Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7074600Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr935,327,31835,329,860
    nsv7074600RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr935,327,31535,329,857

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18783921inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18783921Submitted genomicNC_000009.12:g.353
    27318_35329860inv
    GRCh38 (hg38)NC_000009.12Chr935,327,31835,329,860
    nssv18783921RemappedPerfectNC_000009.11:g.353
    27315_35329857inv
    GRCh37.p13First PassNC_000009.11Chr935,327,31535,329,857

    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)
    nssv187839214e-061276268
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