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nsv4417467

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:397,978

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2875 SVs from 91 studies. See in: genome view    
    Remapped(Score: Perfect):66,401,619-66,799,596Question Mark
    Overlapping variant regions from other studies: 2875 SVs from 91 studies. See in: genome view    
    Submitted genomic68,161,377-68,559,354Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nsv4417467RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1066,401,61966,401,61966,756,96166,799,596
    nsv4417467Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000010.10Chr1068,161,37768,161,37768,516,71968,559,354

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv15716590copy number lossMultipleMultiple

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nssv15716590RemappedPerfectNC_000010.11:g.(66
    401619_66401619)_(
    66756961_66799596)
    del    		GRCh38.p12First PassNC_000010.11Chr1066,401,61966,401,61966,756,96166,799,596
    nssv15716590Submitted genomicNC_000010.10:g.(68
    161377_68161377)_(
    68516719_68559354)
    del    		GRCh37 (hg19)NC_000010.10Chr1068,161,37768,161,37768,516,71968,559,354

    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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