A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2836n100



Internal ID22788923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31960187..32644190hg38UCSC Ensembl
chr16:31971508..32655511hg19UCSC Ensembl
chr16:31879009..32563012hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38684004
hg19684004
hg18684004
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1059842, nsv1065606, nsv1063470, nsv1064648, nsv1059675, nsv1062296, nsv1064971, nsv1066601, nsv1062366, nsv1061721, nsv1064388, nsv1066063, nsv1060423
Samples
Known GenesHERC2P4, LOC390705, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2836n100
Frequency
Sample Size11257
Observed Gain23
Observed Loss0
Observed Complex0
Frequencyn/a


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