A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8427n54



Internal ID22776322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:89265712..89368021hg38UCSC Ensembl
chr3:89314862..89417171hg19UCSC Ensembl
chr3:89397552..89499861hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38102310
hg19102310
hg18102310
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv590922, nsv590923
Samples
Known GenesEPHA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8427n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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