U.S. flag

An official website of the United States government

nsv2733261

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,575,340

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 21641 SVs from 128 studies. See in: genome view    
Remapped(Score: Perfect):103,514,470-112,089,809Question Mark
Overlapping variant regions from other studies: 21648 SVs from 128 studies. See in: genome view    
Remapped(Score: Perfect):103,385,198-111,960,533Question Mark
Overlapping variant regions from other studies: 6445 SVs from 36 studies. See in: genome view    
Submitted genomic102,890,408-111,465,743Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv2733261RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr11103,514,470112,089,809
nsv2733261RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11103,385,198111,960,533
nsv2733261Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000011.8Chr11102,890,408111,465,743

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv13591705deletionSNP arrayProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv13591705RemappedPerfectNC_000011.10:g.(?_
103514470)_(112089
809_?)del
GRCh38.p12First PassNC_000011.10Chr11103,514,470112,089,809
nssv13591705RemappedPerfectNC_000011.9:g.(?_1
03385198)_(1119605
33_?)del
GRCh37.p13First PassNC_000011.9Chr11103,385,198111,960,533
nssv13591705Submitted genomicNC_000011.8:g.(?_1
02890408)_(1114657
43_?)del
NCBI36 (hg18)NC_000011.8Chr11102,890,408111,465,743

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