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nsv4430225

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:707

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 180 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):110,067,914-110,068,620Question Mark
    Overlapping variant regions from other studies: 180 SVs from 47 studies. See in: genome view    
    Submitted genomic112,830,194-112,830,900Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nsv4430225RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr9110,067,914110,067,914110,068,617110,068,620
    nsv4430225Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000009.11Chr9112,830,194112,830,194112,830,897112,830,900

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv15744539copy number lossMultipleMultiple

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nssv15744539RemappedPerfectNC_000009.12:g.(11
    0067914_110067914)
    _(110068617_110068
    620)del    		GRCh38.p12First PassNC_000009.12Chr9110,067,914110,067,914110,068,617110,068,620
    nssv15744539Submitted genomicNC_000009.11:g.(11
    2830194_112830194)
    _(112830897_112830
    900)del    		GRCh37 (hg19)NC_000009.11Chr9112,830,194112,830,194112,830,897112,830,900

    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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