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nsv6715302

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:216,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 655 SVs from 68 studies. See in: genome view    
    Submitted genomic52,656,401-52,872,900Question Mark
    Overlapping variant regions from other studies: 655 SVs from 68 studies. See in: genome view    
    Remapped(Score: Perfect):52,690,417-52,906,916Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6715302Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr352,656,40152,872,900
    nsv6715302RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr352,690,41752,906,916

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18677651duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18677651Submitted genomicNC_000003.12:g.526
    56401_52872900dup
    GRCh38 (hg38)NC_000003.12Chr352,656,40152,872,900
    nssv18677651RemappedPerfectNC_000003.11:g.526
    90417_52906916dup
    GRCh37.p13First PassNC_000003.11Chr352,690,41752,906,916

    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)
    nssv186776512.5e-057271082
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