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nsv4423862

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:340,753

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2298 SVs from 86 studies. See in: genome view    
    Remapped(Score: Perfect):54,928,232-55,268,984Question Mark
    Overlapping variant regions from other studies: 2169 SVs from 83 studies. See in: genome view    
    Submitted genomic54,695,707-55,036,460Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nsv4423862RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1154,928,23254,928,23255,268,98455,268,984
    nsv4423862Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1154,695,70754,701,96154,940,61255,036,460

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv15717949copy number lossMultipleMultiple

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nssv15717949RemappedPerfectNC_000011.10:g.(54
    928232_54928232)_(
    55268984_55268984)
    del    		GRCh38.p12First PassNC_000011.10Chr1154,928,23254,928,23255,268,98455,268,984
    nssv15717949Submitted genomicNC_000011.9:g.(546
    95707_54701961)_(5
    4940612_55036460)d
    el    		GRCh37 (hg19)NC_000011.9Chr1154,695,70754,701,96154,940,61255,036,460

    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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