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nsv6921182

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:17,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 161 SVs from 33 studies. See in: genome view    
    Submitted genomic21,765,301-21,782,500Question Mark
    Overlapping variant regions from other studies: 161 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):21,918,235-21,935,434Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6921182Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1221,765,30121,782,500
    nsv6921182RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1221,918,23521,935,434

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18595736duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18595736Submitted genomicNC_000012.12:g.217
    65301_21782500dup
    GRCh38 (hg38)NC_000012.12Chr1221,765,30121,782,500
    nssv18595736RemappedPerfectNC_000012.11:g.219
    18235_21935434dup
    GRCh37.p13First PassNC_000012.11Chr1221,918,23521,935,434

    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)
    nssv185957361.4e-054275724
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