A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8217n54



Internal ID22776112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8804661..8814440hg38UCSC Ensembl
chr3:8846347..8856126hg19UCSC Ensembl
chr3:8821347..8831126hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg389780
hg199780
hg189780
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv589643, nsv589644
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8217n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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