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nsv4394016

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:36,228

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 296 SVs from 57 studies. See in: genome view    
    Remapped(Score: Perfect):69,619,810-69,656,037Question Mark
    Overlapping variant regions from other studies: 296 SVs from 57 studies. See in: genome view    
    Submitted genomic70,485,528-70,521,755Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nsv4394016RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr469,619,81069,621,65769,651,69569,656,037
    nsv4394016Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000004.11Chr470,485,52870,487,37570,517,41370,521,755

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv15734433copy number lossMultipleMultiple

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nssv15734433RemappedPerfectNC_000004.12:g.(69
    619810_69621657)_(
    69651695_69656037)
    del    		GRCh38.p12First PassNC_000004.12Chr469,619,81069,621,65769,651,69569,656,037
    nssv15734433Submitted genomicNC_000004.11:g.(70
    485528_70487375)_(
    70517413_70521755)
    del    		GRCh37 (hg19)NC_000004.11Chr470,485,52870,487,37570,517,41370,521,755

    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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