A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633679



Internal ID6673800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20210486..20289540hg38UCSC Ensembl
chr14:20678645..20757699hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3879055
hg1979055
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14923763
SamplesHG01462
Known GenesOR11H4, OR11H6, TTC5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633679
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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