A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5101n54



Internal ID20138525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:46380803..46505480hg38UCSC Ensembl
chr16:46385922..46539392hg19UCSC Ensembl
chr16:44943423..45096893hg18UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg38124678
hg19153471
hg18153471
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv572457, nsv572453, nsv572455, nsv572458, nsv572452, nsv572456, nsv572454, nsv572459
Samples
Known GenesANKRD26P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5101n54
Frequency
Sample Size17421
Observed Gain42
Observed Loss0
Observed Complex0
Frequencyn/a


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