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nsv4414868

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,578

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 364 SVs from 67 studies. See in: genome view    
    Remapped(Score: Perfect):114,325,228-114,335,805Question Mark
    Overlapping variant regions from other studies: 364 SVs from 67 studies. See in: genome view    
    Submitted genomic117,087,508-117,098,085Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nsv4414868RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr9114,325,228114,325,257114,332,046114,335,805
    nsv4414868Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000009.11Chr9117,087,508117,087,537117,094,326117,098,085

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv15744587copy number lossMultipleMultiple

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nssv15744587RemappedPerfectNC_000009.12:g.(11
    4325228_114325257)
    _(114332046_114335
    805)del    		GRCh38.p12First PassNC_000009.12Chr9114,325,228114,325,257114,332,046114,335,805
    nssv15744587Submitted genomicNC_000009.11:g.(11
    7087508_117087537)
    _(117094326_117098
    085)del    		GRCh37 (hg19)NC_000009.11Chr9117,087,508117,087,537117,094,326117,098,085

    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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