A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3816n54



Internal ID22771711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:83166272..83253308hg38UCSC Ensembl
chr14:83632616..83719652hg19UCSC Ensembl
chr14:82702369..82789405hg18UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg3887037
hg1987037
hg1887037
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565368, nsv565366
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3816n54
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