A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5011n100



Internal ID22791098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:193149584..193165102hg38UCSC Ensembl
chr3:192867373..192882891hg19UCSC Ensembl
chr3:194350067..194365585hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3815519
hg1915519
hg1815519
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1007407, nsv1005848
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)dgv5011n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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