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nsv7063396

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:31,888

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 273 SVs from 47 studies. See in: genome view    
    Submitted genomic142,372,234-142,404,121Question Mark
    Overlapping variant regions from other studies: 273 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):143,453,595-143,485,482Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7063396Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8142,372,234142,404,121
    nsv7063396RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8143,453,595143,485,482

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18783434inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18783434Submitted genomicNC_000008.11:g.142
    372234_142404121in
    v
    GRCh38 (hg38)NC_000008.11Chr8142,372,234142,404,121
    nssv18783434RemappedPerfectNC_000008.10:g.143
    453595_143485482in
    v
    GRCh37.p13First PassNC_000008.10Chr8143,453,595143,485,482

    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)
    nssv187834344.3e-0512274450
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