A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5136n54



Internal ID22773031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55808492..55829137hg38UCSC Ensembl
chr16:55842404..55863049hg19UCSC Ensembl
chr16:54399905..54420550hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3820646
hg1920646
hg1820646
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv572695, nsv572689, nsv572694
Samples
Known GenesCES1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5136n54
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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