A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1865n54



Internal ID22769760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:54928232..55344108hg38UCSC Ensembl
chr11:54695707..55111584hg19UCSC Ensembl
chr11:54452283..54868160hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38415877
hg19415878
hg18415878
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv554618, nsv554662, nsv554616, nsv554617
Samples
Known GenesOR4A16, TRIM48, TRIM51HP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1865n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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