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nsv6682706

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:197,536

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 401 SVs from 43 studies. See in: genome view    
    Submitted genomic210,069,319-210,266,854Question Mark
    Overlapping variant regions from other studies: 401 SVs from 43 studies. See in: genome view    
    Remapped(Score: Perfect):210,934,043-211,131,578Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6682706Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2210,069,319210,266,854
    nsv6682706RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2210,934,043211,131,578

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18659958duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18659958Submitted genomicNC_000002.12:g.210
    069319_210266854du
    p
    GRCh38 (hg38)NC_000002.12Chr2210,069,319210,266,854
    nssv18659958RemappedPerfectNC_000002.11:g.210
    934043_211131578du
    p
    GRCh37.p13First PassNC_000002.11Chr2210,934,043211,131,578

    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)
    nssv186599587e-062274878
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