A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628138



Internal ID6668282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133065549..133100485hg38UCSC Ensembl
chr11:132935444..132970380hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3834937
hg1934937
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14317797
SamplesNA20763
Known GenesOPCML
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628138
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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