A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2873n100



Internal ID22788960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:32369618..34061880hg38UCSC Ensembl
chr16:32380939..33864347hg19UCSC Ensembl
chr16:32288440..33771848hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381692263
hg191483409
hg181483409
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1067549, nsv1059215, nsv1057228, nsv1065466, nsv1059290, nsv1055720, nsv1056344, nsv1063905, nsv1062058, nsv1065927, nsv1066234, nsv1065745, nsv1057905, nsv1066462, nsv1067332, nsv1056435, nsv1057637, nsv1060835, nsv1063528, nsv1059353, nsv1055869, nsv1063027, nsv1062395, nsv1067375, nsv1066460, nsv1060352, nsv1063318
Samples
Known GenesLOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2873n100
Frequency
Sample Size11257
Observed Gain44
Observed Loss0
Observed Complex0
Frequencyn/a


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