A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2839n100



Internal ID20154455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31960187..33865333hg38UCSC Ensembl
chr16:31971508..33667800hg19UCSC Ensembl
chr16:31879009..33575301hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381905147
hg191696293
hg181696293
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060482, nsv1058780, nsv1067491, nsv1065674, nsv1061079, nsv1056129, nsv1059380, nsv1059392, nsv1060933, nsv1056947, nsv1056813, nsv1064269, nsv1064370, nsv1062421, nsv1058856, nsv1062005, nsv1066307, nsv1066169, nsv1065772, nsv1059104, nsv1060472, nsv1066580, nsv1059179, nsv1067076, nsv1056596, nsv1066253, nsv1066268, nsv1064908, nsv1065856, nsv1067030, nsv1060479, nsv1063424, nsv1056348, nsv1056056, nsv1062675, nsv1064062, nsv1061906, nsv1062526, nsv1059202, nsv1057191
Samples
Known GenesHERC2P4, LOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2839n100
Frequency
Sample Size29084
Observed Gain55
Observed Loss0
Observed Complex0
Frequencyn/a


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