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nsv7033858

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:383

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 117 SVs from 29 studies. See in: genome view    
    Submitted genomic33,743,904-33,744,286Question Mark
    Overlapping variant regions from other studies: 117 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):34,139,891-34,140,273Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7033858Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2233,743,90433,744,286
    nsv7033858RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2234,139,89134,140,273

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18651277duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18651277Submitted genomicNC_000022.11:g.337
    43904_33744286dup
    GRCh38 (hg38)NC_000022.11Chr2233,743,90433,744,286
    nssv18651277RemappedPerfectNC_000022.10:g.341
    39891_34140273dup
    GRCh37.p13First PassNC_000022.10Chr2234,139,89134,140,273

    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)
    nssv186512774e-061226446
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