A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3496n100



Internal ID22789583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:27257073..27474595hg38UCSC Ensembl
chr19:27747981..27965503hg19UCSC Ensembl
chr19:32439821..32657343hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38217523
hg19217523
hg18217523
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1061985, nsv1065630
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)dgv3496n100
Frequency
Sample Size11257
Observed Gain32
Observed Loss0
Observed Complex0
Frequencyn/a


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