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nsv6689824

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:26,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 363 SVs from 64 studies. See in: genome view    
    Submitted genomic208,168,601-208,195,000Question Mark
    Overlapping variant regions from other studies: 363 SVs from 64 studies. See in: genome view    
    Remapped(Score: Perfect):209,033,325-209,059,724Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6689824Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2208,168,601208,195,000
    nsv6689824RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2209,033,325209,059,724

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18448382deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18448382Submitted genomicNC_000002.12:g.208
    168601_208195000de
    l
    GRCh38 (hg38)NC_000002.12Chr2208,168,601208,195,000
    nssv18448382RemappedPerfectNC_000002.11:g.209
    033325_209059724de
    l
    GRCh37.p13First PassNC_000002.11Chr2209,033,325209,059,724

    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)
    nssv18448382<0.001130252614
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