A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5137n54



Internal ID20138561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55808492..55835816hg38UCSC Ensembl
chr16:55842404..55869728hg19UCSC Ensembl
chr16:54399905..54427229hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3827325
hg1927325
hg1827325
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv572691, nsv572692
Samples
Known GenesCES1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5137n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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