A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641959



Internal ID7028730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22521444..22532852hg38UCSC Ensembl
chr18:20101407..20112815hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3811409
hg1911409
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15819542, essv15819545, essv15819540, essv15819544, essv15819543, essv15819541
SamplesHG03619, HG03756, HG03713, HG03634, NA20872, HG01583
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641959
Frequency
Sample Size2504
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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