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nsv6669130

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:447,901

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1555 SVs from 80 studies. See in: genome view    
    Submitted genomic61,348,417-61,796,317Question Mark
    Overlapping variant regions from other studies: 1555 SVs from 80 studies. See in: genome view    
    Remapped(Score: Perfect):61,575,552-62,023,452Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6669130Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr261,348,41761,796,317
    nsv6669130RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr261,575,55262,023,452

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18665945duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18665945Submitted genomicNC_000002.12:g.613
    48417_61796317dup
    GRCh38 (hg38)NC_000002.12Chr261,348,41761,796,317
    nssv18665945RemappedPerfectNC_000002.11:g.615
    75552_62023452dup
    GRCh37.p13First PassNC_000002.11Chr261,575,55262,023,452

    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)
    nssv186659454e-061275968
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