A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4688n100



Internal ID22790775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21052242..21200164hg38UCSC Ensembl
chr3:21093734..21241656hg19UCSC Ensembl
chr3:21068738..21216660hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38147923
hg19147923
hg18147923
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1012561, nsv1003715
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)dgv4688n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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