nsv6701616

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:72,485

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 807 SVs from 86 studies. See in: genome view    
    Submitted genomic240,613,471-240,685,955Question Mark
    Overlapping variant regions from other studies: 807 SVs from 86 studies. See in: genome view    
    Remapped(Score: Perfect):241,552,888-241,625,372Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6701616Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2240,613,471240,685,955
    nsv6701616RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2241,552,888241,625,372

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18664380duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18664380Submitted genomicNC_000002.12:g.240
    613471_240685955du
    p
    GRCh38 (hg38)NC_000002.12Chr2240,613,471240,685,955
    nssv18664380RemappedPerfectNC_000002.11:g.241
    552888_241625372du
    p
    GRCh37.p13First PassNC_000002.11Chr2241,552,888241,625,372

    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)
    nssv186643804e-061274746
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