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nsv6681715

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:167

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 100 SVs from 24 studies. See in: genome view    
    Submitted genomic228,542,384-228,542,550Question Mark
    Overlapping variant regions from other studies: 100 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):229,407,100-229,407,266Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6681715Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2228,542,384228,542,550
    nsv6681715RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2229,407,100229,407,266

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18662058duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18662058Submitted genomicNC_000002.12:g.228
    542384_228542550du
    p
    GRCh38 (hg38)NC_000002.12Chr2228,542,384228,542,550
    nssv18662058RemappedPerfectNC_000002.11:g.229
    407100_229407266du
    p
    GRCh37.p13First PassNC_000002.11Chr2229,407,100229,407,266

    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)
    nssv18662058<0.00165226968
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