A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2065n54



Internal ID20135489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:89231351..89234610hg38UCSC Ensembl
chr11:88964519..88967778hg19UCSC Ensembl
chr11:88604167..88607426hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg383260
hg193260
hg183260
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv555753, nsv555749, nsv555748, nsv555750, nsv555755, nsv555756, nsv555747
Samples
Known GenesTYR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2065n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss32
Observed Complex0
Frequencyn/a


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