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nsv7026920

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,768

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 195 SVs from 47 studies. See in: genome view    
    Submitted genomic63,946,557-63,954,324Question Mark
    Overlapping variant regions from other studies: 195 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):62,577,910-62,585,677Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7026920Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2063,946,55763,954,324
    nsv7026920RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2062,577,91062,585,677

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18643812duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18643812Submitted genomicNC_000020.11:g.639
    46557_63954324dup
    GRCh38 (hg38)NC_000020.11Chr2063,946,55763,954,324
    nssv18643812RemappedPerfectNC_000020.10:g.625
    77910_62585677dup
    GRCh37.p13First PassNC_000020.10Chr2062,577,91062,585,677

    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)
    nssv186438127e-062273648
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