A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8610n54



Internal ID20142034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133573902..133574696hg38UCSC Ensembl
chr3:133292746..133293540hg19UCSC Ensembl
chr3:134775436..134776230hg18UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38795
hg19795
hg18795
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv591824, nsv591827, nsv591825, nsv591826
Samples
Known GenesCDV3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8610n54
Frequency
Sample Size17421
Observed Gain18
Observed Loss0
Observed Complex0
Frequencyn/a


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