A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556470



Internal ID15997193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:119350236..119376186hg38UCSC Ensembl
Innerchr11:119220946..119246896hg19UCSC Ensembl
Innerchr11:118726156..118752106hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3825951
hg1925951
hg1825951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv784615
Samples
Known GenesUSP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556470
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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