A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4650n100



Internal ID20156266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4079539..4189324hg38UCSC Ensembl
chr3:4121223..4231008hg19UCSC Ensembl
chr3:4096223..4206008hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38109786
hg19109786
hg18109786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1008526, nsv998686
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)dgv4650n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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