A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8168n54



Internal ID20141592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2454047..2454809hg38UCSC Ensembl
chr3:2495731..2496493hg19UCSC Ensembl
chr3:2470731..2471493hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38763
hg19763
hg18763
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv589383, nsv589384, nsv589382, nsv589385
Samples
Known GenesCNTN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8168n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss64
Observed Complex0
Frequencyn/a


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