A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8428n54



Internal ID22776323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:89326283..89369112hg38UCSC Ensembl
chr3:89375433..89418262hg19UCSC Ensembl
chr3:89458123..89500952hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3842830
hg1942830
hg1842830
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv590924, nsv590927, nsv590925, nsv590926
Samples
Known GenesEPHA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8428n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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