A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3436n100



Internal ID20155052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12451697..12597468hg38UCSC Ensembl
chr19:12562511..12708282hg19UCSC Ensembl
chr19:12423511..12569282hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38145772
hg19145772
hg18145772
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1065773, nsv1057869, nsv1060358, nsv1066784, nsv1062216
Samples
Known GenesZNF490, ZNF564, ZNF709
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3436n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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