nsv6701712

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:170,462

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 389 SVs from 47 studies. See in: genome view    
    Submitted genomic57,231,818-57,402,279Question Mark
    Overlapping variant regions from other studies: 309 SVs from 44 studies. See in: genome view    
    Remapped(Score: Pass):57,265,846-57,369,477Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6701712Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr357,231,81857,402,279
    nsv6701712RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr357,265,84657,369,477

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18677770duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18677770Submitted genomicNC_000003.12:g.572
    31818_57402279dup
    GRCh38 (hg38)NC_000003.12Chr357,231,81857,402,279
    nssv18677770RemappedPassNC_000003.11:g.572
    65846_57369477dup
    GRCh37.p13First PassNC_000003.11Chr357,265,84657,369,477

    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)
    nssv186777707e-062273242
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