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nsv7059980

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,204,915

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 8474 SVs from 107 studies. See in: genome view    
    Submitted genomic30,656,049-33,860,963Question Mark
    Overlapping variant regions from other studies: 7731 SVs from 104 studies. See in: genome view    
    Remapped(Score: Pass):29,803,910-32,448,769Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7059980Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2030,656,04933,860,963
    nsv7059980RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2029,803,91032,448,769

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18762262inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18762262Submitted genomicNC_000020.11:g.306
    56049_33860963inv
    GRCh38 (hg38)NC_000020.11Chr2030,656,04933,860,963
    nssv18762262RemappedPassNC_000020.10:g.298
    03910_32448769inv
    GRCh37.p13First PassNC_000020.10Chr2029,803,91032,448,769

    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)
    nssv187622621.1e-053275354
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