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nsv6674767

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:389

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 91 SVs from 16 studies. See in: genome view    
    Submitted genomic14,327,185-14,327,573Question Mark
    Overlapping variant regions from other studies: 91 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):14,467,309-14,467,697Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6674767Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr214,327,18514,327,573
    nsv6674767RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr214,467,30914,467,697

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18650150duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18650150Submitted genomicNC_000002.12:g.143
    27185_14327573dup
    GRCh38 (hg38)NC_000002.12Chr214,327,18514,327,573
    nssv18650150RemappedPerfectNC_000002.11:g.144
    67309_14467697dup
    GRCh37.p13First PassNC_000002.11Chr214,467,30914,467,697

    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)
    nssv186501508e-062241496
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