A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626981



Internal ID7013811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82086863..82145527hg38UCSC Ensembl
chr11:81797905..81856569hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3858665
hg1958665
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14218109
SamplesHG03304
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626981
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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