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nsv6941433

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:73,568

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 297 SVs from 45 studies. See in: genome view    
    Submitted genomic42,766,420-42,839,987Question Mark
    Overlapping variant regions from other studies: 297 SVs from 45 studies. See in: genome view    
    Remapped(Score: Perfect):43,340,556-43,414,123Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6941433Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1342,766,42042,839,987
    nsv6941433RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1343,340,55643,414,123

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18604243duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18604243Submitted genomicNC_000013.11:g.427
    66420_42839987dup
    GRCh38 (hg38)NC_000013.11Chr1342,766,42042,839,987
    nssv18604243RemappedPerfectNC_000013.10:g.433
    40556_43414123dup
    GRCh37.p13First PassNC_000013.10Chr1343,340,55643,414,123

    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)
    nssv186042431.1e-053275100
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