A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8374n54



Internal ID20141798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71753521..71754987hg38UCSC Ensembl
chr3:71802672..71804138hg19UCSC Ensembl
chr3:71885362..71886828hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381467
hg191467
hg181467
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv590607, nsv590609, nsv590608
Samples
Known GenesEIF4E3, GPR27
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8374n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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