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nsv7065076

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:21,607

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 522 SVs from 49 studies. See in: genome view    
    Submitted genomic50,737,291-50,758,897Question Mark
    Overlapping variant regions from other studies: 521 SVs from 49 studies. See in: genome view    
    Remapped(Score: Perfect):51,175,719-51,197,325Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7065076Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2250,737,29150,758,897
    nsv7065076RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2251,175,71951,197,325

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18763617inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18763617Submitted genomicNC_000022.11:g.507
    37291_50758897inv
    GRCh38 (hg38)NC_000022.11Chr2250,737,29150,758,897
    nssv18763617RemappedPerfectNC_000022.10:g.511
    75719_51197325inv
    GRCh37.p13First PassNC_000022.10Chr2251,175,71951,197,325

    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)
    nssv187636171.1e-053274668
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