U.S. flag

An official website of the United States government

nsv6620799

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:65,539

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 214 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):113,942,991-114,008,529Question Mark
Overlapping variant regions from other studies: 214 SVs from 32 studies. See in: genome view    
Submitted genomic113,813,713-113,879,251Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv6620799RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr11113,942,991114,008,529
nsv6620799Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr11113,813,713113,879,251

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv18292531duplicationOSC3882SNP arrayProbe signal intensity8

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv18292531RemappedPerfectNC_000011.10:g.(?_
113942991)_(114008
529_?)dup
GRCh38.p12First PassNC_000011.10Chr11113,942,991114,008,529
nssv18292531Submitted genomicNC_000011.9:g.(?_1
13813713)_(1138792
51_?)dup
GRCh37 (hg19)NC_000011.9Chr11113,813,713113,879,251

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

Support Center