A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv763575



Internal ID16057531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:836971..839155hg38UCSC Ensembl
Innerchr11:836971..839155hg19UCSC Ensembl
Innerchr11:826971..829155hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg382185
hg192185
hg182185
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552880
Supporting Variants
Samples
Known GenesCD151
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv763575
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