A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638874



Internal ID7025659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66940449..67019762hg38UCSC Ensembl
chr16:66974352..67053665hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3879314
hg1979314
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv526e214
Supporting Variantsessv15501379, essv15501377, essv15501378
SamplesHG03976, HG03696, HG03848
Known GenesCES2, CES3, CES4A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638874
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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