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nsv6131906

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:70,002

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 240 SVs from 48 studies. See in: genome view    
    Remapped(Score: Perfect):102,769,269-102,839,270Question Mark
    Overlapping variant regions from other studies: 240 SVs from 48 studies. See in: genome view    
    Submitted genomic102,640,000-102,710,001Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6131906RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr11102,769,269102,839,270
    nsv6131906Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr11102,640,000102,710,001

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
    nssv17679306copy number gainSAMN20524657SequencingPaired-end mapping656

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17679306RemappedPerfectNC_000011.10:g.102
    769269_102839270du
    p
    GRCh38.p12First PassNC_000011.10Chr11102,769,269102,839,270
    nssv17679306Submitted genomicNC_000011.9:g.1026
    40000_102710001dup
    GRCh37 (hg19)NC_000011.9Chr11102,640,000102,710,001

    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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