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nsv6682364

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:63,778

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 269 SVs from 40 studies. See in: genome view    
    Submitted genomic196,872,903-196,936,680Question Mark
    Overlapping variant regions from other studies: 269 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):197,737,627-197,801,404Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6682364Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2196,872,903196,936,680
    nsv6682364RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2197,737,627197,801,404

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18658810duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18658810Submitted genomicNC_000002.12:g.196
    872903_196936680du
    p
    GRCh38 (hg38)NC_000002.12Chr2196,872,903196,936,680
    nssv18658810RemappedPerfectNC_000002.11:g.197
    737627_197801404du
    p
    GRCh37.p13First PassNC_000002.11Chr2197,737,627197,801,404

    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)
    nssv186588107e-062275024
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