A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552876



Internal ID15993599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:830234..831809hg38UCSC Ensembl
Innerchr11:830234..831809hg19UCSC Ensembl
Innerchr11:820234..821809hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381576
hg191576
hg181576
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv763571
Samples
Known GenesEFCAB4A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552876
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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