A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553464



Internal ID16340873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:9302339..9313414hg38UCSC Ensembl
Innerchr11:9323886..9334961hg19UCSC Ensembl
Innerchr11:9280462..9291537hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3811076
hg1911076
hg1811076
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv767225
Samples
Known GenesTMEM41B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553464
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer