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nsv6685718

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,360

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 167 SVs from 28 studies. See in: genome view    
    Submitted genomic196,830,093-196,838,452Question Mark
    Overlapping variant regions from other studies: 167 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):197,694,817-197,703,176Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6685718Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2196,830,093196,838,452
    nsv6685718RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2197,694,817197,703,176

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18658807duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18658807Submitted genomicNC_000002.12:g.196
    830093_196838452du
    p
    GRCh38 (hg38)NC_000002.12Chr2196,830,093196,838,452
    nssv18658807RemappedPerfectNC_000002.11:g.197
    694817_197703176du
    p
    GRCh37.p13First PassNC_000002.11Chr2197,694,817197,703,176

    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)
    nssv186588072.1e-056274558
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