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nsv6133741

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,090,002

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 8157 SVs from 113 studies. See in: genome view    
    Remapped(Score: Perfect):158,420,210-161,510,211Question Mark
    Overlapping variant regions from other studies: 8161 SVs from 113 studies. See in: genome view    
    Submitted genomic158,390,000-161,480,001Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6133741RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1158,420,210161,510,211
    nsv6133741Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr1158,390,000161,480,001

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
    nssv17677589copy number gainSAMN20524654SequencingPaired-end mapping440

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17677589RemappedPerfectNC_000001.11:g.158
    420210_161510211du
    p
    GRCh38.p12First PassNC_000001.11Chr1158,420,210161,510,211
    nssv17677589Submitted genomicNC_000001.10:g.158
    390000_161480001du
    p
    GRCh37 (hg19)NC_000001.10Chr1158,390,000161,480,001

    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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