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nsv6136851

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:710,002

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2056 SVs from 83 studies. See in: genome view    
    Remapped(Score: Perfect):94,437,718-95,147,719Question Mark
    Overlapping variant regions from other studies: 2056 SVs from 83 studies. See in: genome view    
    Submitted genomic97,200,000-97,910,001Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6136851RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr994,437,71895,147,719
    nsv6136851Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000009.11Chr997,200,00097,910,001

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
    nssv17677995copy number gainSAMN20524663SequencingPaired-end mapping244

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17677995RemappedPerfectNC_000009.12:g.944
    37718_95147719dup
    GRCh38.p12First PassNC_000009.12Chr994,437,71895,147,719
    nssv17677995Submitted genomicNC_000009.11:g.972
    00000_97910001dup
    GRCh37 (hg19)NC_000009.11Chr997,200,00097,910,001

    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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