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nsv4428879

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:17,749

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 331 SVs from 65 studies. See in: genome view    
    Remapped(Score: Perfect):104,601,540-104,619,288Question Mark
    Overlapping variant regions from other studies: 331 SVs from 65 studies. See in: genome view    
    Submitted genomic107,363,821-107,381,569Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nsv4428879RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr9104,601,540104,604,600104,617,358104,619,288
    nsv4428879Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000009.11Chr9107,363,821107,366,881107,379,639107,381,569

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv15744491copy number lossMultipleMultiple

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nssv15744491RemappedPerfectNC_000009.12:g.(10
    4601540_104604600)
    _(104617358_104619
    288)del    		GRCh38.p12First PassNC_000009.12Chr9104,601,540104,604,600104,617,358104,619,288
    nssv15744491Submitted genomicNC_000009.11:g.(10
    7363821_107366881)
    _(107379639_107381
    569)del    		GRCh37 (hg19)NC_000009.11Chr9107,363,821107,366,881107,379,639107,381,569

    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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