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nsv6133932

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:320,002

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 694 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):160,310,210-160,630,211Question Mark
    Overlapping variant regions from other studies: 698 SVs from 55 studies. See in: genome view    
    Submitted genomic160,280,000-160,600,001Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6133932RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1160,310,210160,630,211
    nsv6133932Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr1160,280,000160,600,001

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
    nssv17677864copy number gainSAMN20524657SequencingPaired-end mapping656

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17677864RemappedPerfectNC_000001.11:g.160
    310210_160630211du
    p
    GRCh38.p12First PassNC_000001.11Chr1160,310,210160,630,211
    nssv17677864Submitted genomicNC_000001.10:g.160
    280000_160600001du
    p
    GRCh37 (hg19)NC_000001.10Chr1160,280,000160,600,001

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    No genotype data were submitted for this variant

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