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nsv4414957

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,048

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 234 SVs from 45 studies. See in: genome view    
    Remapped(Score: Perfect):129,763,416-129,768,463Question Mark
    Overlapping variant regions from other studies: 234 SVs from 45 studies. See in: genome view    
    Submitted genomic132,525,695-132,530,742Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nsv4414957RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr9129,763,416129,764,025129,768,252129,768,463
    nsv4414957Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000009.11Chr9132,525,695132,526,304132,530,531132,530,742

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv15744737copy number lossMultipleMultiple

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nssv15744737RemappedPerfectNC_000009.12:g.(12
    9763416_129764025)
    _(129768252_129768
    463)del    		GRCh38.p12First PassNC_000009.12Chr9129,763,416129,764,025129,768,252129,768,463
    nssv15744737Submitted genomicNC_000009.11:g.(13
    2525695_132526304)
    _(132530531_132530
    742)del    		GRCh37 (hg19)NC_000009.11Chr9132,525,695132,526,304132,530,531132,530,742

    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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