A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626326



Internal ID6666475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:49889223..50083546hg38UCSC Ensembl
chr11:49910775..50042705hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38194324
hg19131931
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14144695
SamplesNA20761
Known GenesOR4C12, OR4C13
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626326
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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