A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3432n100



Internal ID22789519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12391388..12438841hg38UCSC Ensembl
chr19:12502202..12549655hg19UCSC Ensembl
chr19:12363202..12410655hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3847454
hg1947454
hg1847454
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1057201, nsv1057691, nsv1060516, nsv1055540, nsv1060950
Samples
Known GenesZNF443, ZNF799
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3432n100
Frequency
Sample Size11257
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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