A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv180e214



Internal ID22756074
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 Variants
Supporting Variantsesv3625183, esv3625181
SamplesHG03687, HG00261, HG01892, HG03779
Known GenesOR52B4, OR52K2, TRIM21
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv180e214
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer