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nsv594311

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,850

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 267 SVs from 58 studies. See in: genome view    
Remapped(Score: Perfect):61,074,287-61,082,136Question Mark
Overlapping variant regions from other studies: 267 SVs from 58 studies. See in: genome view    
Remapped(Score: Perfect):61,940,005-61,947,854Question Mark
Overlapping variant regions from other studies: 131 SVs from 20 studies. See in: genome view    
Submitted genomic61,622,600-61,630,449Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv594311RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr461,074,28761,082,136
nsv594311RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr461,940,00561,947,854
nsv594311Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000004.10Chr461,622,60061,630,449

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv999467copy number gainSNP arraySNP genotyping analysis

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv999467RemappedPerfectNC_000004.12:g.(?_
61074287)_(6108213
6_?)dup
GRCh38.p12First PassNC_000004.12Chr461,074,28761,082,136
nssv999467RemappedPerfectNC_000004.11:g.(?_
61940005)_(6194785
4_?)dup
GRCh37.p13First PassNC_000004.11Chr461,940,00561,947,854
nssv999467Submitted genomicNC_000004.10:g.(?_
61622600)_(6163044
9_?)dup
NCBI36 (hg18)NC_000004.10Chr461,622,60061,630,449

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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