A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788638



Internal ID19170517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105585928..105708865hg38UCSC Ensembl
Innerchr14:106052265..106175202hg19UCSC Ensembl
Innerchr14:105123310..105246247hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38122938
hg19122938
hg18122938
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892587
Supporting Variants
Samples
Known GenesELK2AP, MIR8071-1, MIR8071-2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788638
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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