A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv774853



Internal ID15722123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55009318..55336141hg38UCSC Ensembl
Innerchr11:54776794..55103617hg19UCSC Ensembl
Innerchr11:54533370..54860193hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38326824
hg19326824
hg18326824
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554662
Supporting Variants
Samples
Known GenesTRIM48, TRIM51HP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv774853
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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