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nsv6931489

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:494,414

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1612 SVs from 81 studies. See in: genome view    
    Submitted genomic52,539,483-53,033,896Question Mark
    Overlapping variant regions from other studies: 1612 SVs from 81 studies. See in: genome view    
    Remapped(Score: Perfect):52,933,267-53,427,680Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6931489Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1252,539,48353,033,896
    nsv6931489RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1252,933,26753,427,680

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18595370duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18595370Submitted genomicNC_000012.12:g.525
    39483_53033896dup
    GRCh38 (hg38)NC_000012.12Chr1252,539,48353,033,896
    nssv18595370RemappedPerfectNC_000012.11:g.529
    33267_53427680dup
    GRCh37.p13First PassNC_000012.11Chr1252,933,26753,427,680

    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)
    nssv185953704e-061275618
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