A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2845n100



Internal ID22788932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:32022053..32481160hg38UCSC Ensembl
chr16:32033374..32492481hg19UCSC Ensembl
chr16:31940875..32399982hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38459108
hg19459108
hg18459108
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1064416, nsv1059653, nsv1057716, nsv1067284, nsv1062547
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)dgv2845n100
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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