A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3467n100



Internal ID20155083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20618903..20815171hg38UCSC Ensembl
chr19:20801709..20997977hg19UCSC Ensembl
chr19:20593549..20789817hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38196269
hg19196269
hg18196269
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1064916, nsv1056879, nsv1060579, nsv1067183, nsv1059582, nsv1063556, nsv1066747, nsv1067256, nsv1056551, nsv1066131, nsv1060259, nsv1065615, nsv1060429, nsv1058458, nsv1065039, nsv1055911, nsv1065960, nsv1065495, nsv1063760, nsv1061028, nsv1061771, nsv1062051, nsv1061596
Samples
Known GenesZNF626
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3467n100
Frequency
Sample Size29084
Observed Gain53
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer