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nsv7068293

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,921,967

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 22819 SVs from 128 studies. See in: genome view    
    Submitted genomic12,453,912-21,375,878Question Mark
    Overlapping variant regions from other studies: 22827 SVs from 128 studies. See in: genome view    
    Remapped(Score: Perfect):12,453,912-21,375,877Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7068293Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr912,453,91221,375,878
    nsv7068293RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr912,453,91221,375,877

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18784356inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18784356Submitted genomicNC_000009.12:g.124
    53912_21375878inv
    GRCh38 (hg38)NC_000009.12Chr912,453,91221,375,878
    nssv18784356RemappedPerfectNC_000009.11:g.124
    53912_21375877inv
    GRCh37.p13First PassNC_000009.11Chr912,453,91221,375,877

    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)
    nssv187843564e-061276268
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