A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14918891



Internal ID5818068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:19867394..19955157hg38UCSC Ensembl
chr14:20335553..20423316hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3887764
hg1987764
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633663
Supporting Variants
SamplesNA19197
Known GenesOR4K1, OR4K2, OR4K5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14918891
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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