A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8154n54



Internal ID20141578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:768195..1386951hg38UCSC Ensembl
chr3:809878..1428635hg19UCSC Ensembl
chr3:784878..1403635hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38618757
hg19618758
hg18618758
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv589302, nsv589307, nsv589305, nsv589304, nsv589306, nsv589303
Samples
Known GenesCNTN6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8154n54
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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