A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1566n54



Internal ID22769461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2155622..2160036hg38UCSC Ensembl
chr11:2176852..2181266hg19UCSC Ensembl
chr11:2133428..2137842hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg384415
hg194415
hg184415
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553072, nsv553073
Samples
Known GenesINS, INS-IGF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1566n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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