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nsv4411969

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:293,115

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3715 SVs from 103 studies. See in: genome view    
    Remapped(Score: Perfect):11,735,515-12,028,629Question Mark
    Overlapping variant regions from other studies: 3719 SVs from 103 studies. See in: genome view    
    Submitted genomic11,735,515-12,028,629Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nsv4411969RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr911,735,51511,839,01212,021,34512,028,629
    nsv4411969Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000009.11Chr911,735,51511,839,01212,021,34512,028,629

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv15743503copy number lossMultipleMultiple

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nssv15743503RemappedPerfectNC_000009.12:g.(11
    735515_11839012)_(
    12021345_12028629)
    del    		GRCh38.p12First PassNC_000009.12Chr911,735,51511,839,01212,021,34512,028,629
    nssv15743503Submitted genomicNC_000009.11:g.(11
    735515_11839012)_(
    12021345_12028629)
    del    		GRCh37 (hg19)NC_000009.11Chr911,735,51511,839,01212,021,34512,028,629

    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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