A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14923763



Internal ID4925579
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633679
Supporting Variants
SamplesHG01462
Known GenesOR11H4, OR11H6, TTC5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14923763
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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