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nsv6132408

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:190,002

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 631 SVs from 63 studies. See in: genome view    
    Remapped(Score: Perfect):113,312,195-113,502,196Question Mark
    Overlapping variant regions from other studies: 631 SVs from 63 studies. See in: genome view    
    Submitted genomic113,750,000-113,940,001Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6132408RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr12113,312,195113,502,196
    nsv6132408Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000012.11Chr12113,750,000113,940,001

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
    nssv17679794copy number gainSAMN20524654SequencingPaired-end mapping440

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17679794RemappedPerfectNC_000012.12:g.113
    312195_113502196du
    p
    GRCh38.p12First PassNC_000012.12Chr12113,312,195113,502,196
    nssv17679794Submitted genomicNC_000012.11:g.113
    750000_113940001du
    p
    GRCh37 (hg19)NC_000012.11Chr12113,750,000113,940,001

    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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