A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1658n54



Internal ID18993834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13276938..13277953hg38UCSC Ensembl
chr11:13298485..13299500hg19UCSC Ensembl
chr11:13255061..13256076hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg381016
hg191016
hg181016
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553550, nsv553551
Samples
Known GenesARNTL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1658n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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