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nsv6661296

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:78

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 133 SVs from 21 studies. See in: genome view    
    Submitted genomic209,629,834-209,629,911Question Mark
    Overlapping variant regions from other studies: 137 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):209,803,179-209,803,256Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6661296Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1209,629,834209,629,911
    nsv6661296RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1209,803,179209,803,256

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18608390duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18608390Submitted genomicNC_000001.11:g.209
    629834_209629911du
    p
    GRCh38 (hg38)NC_000001.11Chr1209,629,834209,629,911
    nssv18608390RemappedPerfectNC_000001.10:g.209
    803179_209803256du
    p
    GRCh37.p13First PassNC_000001.10Chr1209,803,179209,803,256

    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)
    nssv18608390<0.00177220758
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