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nsv7039556

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:492,507

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1581 SVs from 96 studies. See in: genome view    
    Submitted genomic192,908,987-193,401,493Question Mark
    Overlapping variant regions from other studies: 1581 SVs from 96 studies. See in: genome view    
    Remapped(Score: Perfect):192,626,776-193,119,282Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7039556Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3192,908,987193,401,493
    nsv7039556RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3192,626,776193,119,282

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18770919inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18770919Submitted genomicNC_000003.12:g.192
    908987_193401493in
    v
    GRCh38 (hg38)NC_000003.12Chr3192,908,987193,401,493
    nssv18770919RemappedPerfectNC_000003.11:g.192
    626776_193119282in
    v
    GRCh37.p13First PassNC_000003.11Chr3192,626,776193,119,282

    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)
    nssv187709191.1e-053271650
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