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nsv6134795

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,470,002

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3475 SVs from 85 studies. See in: genome view    
    Remapped(Score: Perfect):179,222,212-180,692,213Question Mark
    Overlapping variant regions from other studies: 3475 SVs from 85 studies. See in: genome view    
    Submitted genomic178,940,000-180,410,001Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6134795RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3179,222,212180,692,213
    nsv6134795Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3178,940,000180,410,001

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
    nssv17679030copy number gainSAMN20524660SequencingPaired-end mapping208

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17679030RemappedPerfectNC_000003.12:g.179
    222212_180692213du
    p
    GRCh38.p12First PassNC_000003.12Chr3179,222,212180,692,213
    nssv17679030Submitted genomicNC_000003.11:g.178
    940000_180410001du
    p
    GRCh37 (hg19)NC_000003.11Chr3178,940,000180,410,001

    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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