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nsv7023452

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:48,619

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 238 SVs from 42 studies. See in: genome view    
    Submitted genomic41,183,197-41,231,815Question Mark
    Overlapping variant regions from other studies: 238 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):41,579,201-41,627,819Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7023452Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2241,183,19741,231,815
    nsv7023452RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2241,579,20141,627,819

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18653025duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18653025Submitted genomicNC_000022.11:g.411
    83197_41231815dup
    GRCh38 (hg38)NC_000022.11Chr2241,183,19741,231,815
    nssv18653025RemappedPerfectNC_000022.10:g.415
    79201_41627819dup
    GRCh37.p13First PassNC_000022.10Chr2241,579,20141,627,819

    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)
    nssv186530252.2e-056272370
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