A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2185n54



Internal ID20135609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116865227..116866285hg38UCSC Ensembl
chr11:116735943..116737001hg19UCSC Ensembl
chr11:116241153..116242211hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381059
hg191059
hg181059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556453, nsv556452
Samples
Known GenesSIK3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2185n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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