A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4679n100



Internal ID20156295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8777881..8830534hg38UCSC Ensembl
chr3:8819567..8872219hg19UCSC Ensembl
chr3:8794567..8847219hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3852654
hg1952653
hg1852653
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv998743, nsv1014057, nsv1008589
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4679n100
Frequency
Sample Size29084
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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