A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626177



Internal ID7013011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45759499..45769059hg38UCSC Ensembl
chr11:45781050..45790610hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg389561
hg199561
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14118536
SamplesHG01608
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626177
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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