A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4673n100



Internal ID20156289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:6648983..6782709hg38UCSC Ensembl
chr3:6690670..6824396hg19UCSC Ensembl
chr3:6665670..6799396hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38133727
hg19133727
hg18133727
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1012776, nsv1001310
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)dgv4673n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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