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nsv1037810

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:225,868

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 853 SVs from 92 studies. See in: genome view    
Remapped(Score: Perfect):67,743,143-67,969,010Question Mark
Overlapping variant regions from other studies: 849 SVs from 92 studies. See in: genome view    
Remapped(Score: Perfect):67,510,614-67,736,481Question Mark
Overlapping variant regions from other studies: 265 SVs from 25 studies. See in: genome view    
Submitted genomic67,267,190-67,493,057Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv1037810RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1167,743,14367,969,010
nsv1037810RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1167,510,61467,736,481
nsv1037810Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000011.8Chr1167,267,19067,493,057

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv3504316copy number lossSNP arrayProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv3504316RemappedPerfectNC_000011.10:g.(?_
67743143)_(6796901
0_?)del
GRCh38.p12First PassNC_000011.10Chr1167,743,14367,969,010
nssv3504316RemappedPerfectNC_000011.9:g.(?_6
7510614)_(67736481
_?)del
GRCh37.p13First PassNC_000011.9Chr1167,510,61467,736,481
nssv3504316Submitted genomicNC_000011.8:g.(?_6
7267190)_(67493057
_?)del
NCBI36 (hg18)NC_000011.8Chr1167,267,19067,493,057

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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