A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552880



Internal ID16340289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:836971..839155hg38UCSC Ensembl
Innerchr11:836971..839155hg19UCSC Ensembl
Innerchr11:826971..829155hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg382185
hg192185
hg182185
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv763575
Samples
Known GenesCD151
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552880
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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