A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3998n54



Internal ID20137422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105474495..105770768hg38UCSC Ensembl
chr14:105940832..106237105hg19UCSC Ensembl
chr14:105011877..105308150hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38296274
hg19296274
hg18296274
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv566273, nsv566261
Samples
Known GenesC14orf80, CRIP1, CRIP2, ELK2AP, MIR8071-1, MIR8071-2, TMEM121
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3998n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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