A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554866



Internal ID15995589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55602849..55647930hg38UCSC Ensembl
Innerchr11:55370325..55415406hg19UCSC Ensembl
Innerchr11:55126901..55171982hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3845082
hg1945082
hg1845082
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1914n54
Supporting Variantsnssv775927
Samples
Known GenesOR4C11, OR4P4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554866
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