A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625181



Internal ID7012016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4366754..4450243hg38UCSC Ensembl
chr11:4387984..4471473hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3883490
hg1983490
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv180e214
Supporting Variantsessv13998739, essv13998738, essv13998740
SamplesHG03687, HG00261, HG03779
Known GenesOR52B4, OR52K2, TRIM21
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625181
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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