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nsv7019967

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 214 SVs from 26 studies. See in: genome view    
    Submitted genomic43,774,771-43,774,970Question Mark
    Overlapping variant regions from other studies: 214 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):45,194,652-45,194,851Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7019967Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2143,774,77143,774,970
    nsv7019967RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2145,194,65245,194,851

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18644139duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18644139Submitted genomicNC_000021.9:g.4377
    4771_43774970dup
    GRCh38 (hg38)NC_000021.9Chr2143,774,77143,774,970
    nssv18644139RemappedPerfectNC_000021.8:g.4519
    4652_45194851dup
    GRCh37.p13First PassNC_000021.8Chr2145,194,65245,194,851

    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)
    nssv186441398e-062238750
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