nsv4425398

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:674,797

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 5028 SVs from 97 studies. See in: genome view    
    Remapped(Score: Good):21,861,568-22,536,364Question Mark
    Overlapping variant regions from other studies: 5186 SVs from 102 studies. See in: genome view    
    Submitted genomic22,329,745-23,005,311Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nsv4425398RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000014.9Chr1421,861,56821,861,56822,536,36422,536,364
    nsv4425398Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000014.8Chr1422,329,74522,372,27323,000,25623,005,311

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv15721319copy number lossMultipleMultiple

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nssv15721319RemappedGoodNC_000014.9:g.(218
    61568_21861568)_(2
    2536364_22536364)d
    el    		GRCh38.p12First PassNC_000014.9Chr1421,861,56821,861,56822,536,36422,536,364
    nssv15721319Submitted genomicNC_000014.8:g.(223
    29745_22372273)_(2
    3000256_23005311)d
    el    		GRCh37 (hg19)NC_000014.8Chr1422,329,74522,372,27323,000,25623,005,311

    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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