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nsv6134077

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:111,804

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 699 SVs from 89 studies. See in: genome view    
    Remapped(Score: Perfect):128,792,297-128,904,100Question Mark
    Overlapping variant regions from other studies: 699 SVs from 89 studies. See in: genome view    
    Submitted genomic129,549,871-129,661,674Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nsv6134077RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2128,792,297128,792,301128,904,097128,904,100
    nsv6134077Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr2129,549,871129,549,875129,661,671129,661,674

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
    nssv17682051duplicationSAMN20524659SequencingPaired-end mapping203

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nssv17682051RemappedPerfectNC_000002.12:g.(12
    8792297_128792301)
    _(128904097_128904
    100)dup    		GRCh38.p12First PassNC_000002.12Chr2128,792,297128,792,301128,904,097128,904,100
    nssv17682051Submitted genomicNC_000002.11:g.(12
    9549871_129549875)
    _(129661671_129661
    674)dup    		GRCh37 (hg19)NC_000002.11Chr2129,549,871129,549,875129,661,671129,661,674

    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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