A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3434n100



Internal ID22789521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12405336..12438841hg38UCSC Ensembl
chr19:12516150..12549655hg19UCSC Ensembl
chr19:12377150..12410655hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3833506
hg1933506
hg1833506
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1055348, nsv1059474, nsv1064578, nsv1055275, nsv1065779, nsv1067414, nsv1056181
Samples
Known GenesZNF443
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3434n100
Frequency
Sample Size11257
Observed Gain30
Observed Loss0
Observed Complex0
Frequencyn/a


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