A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554871



Internal ID15995594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55602849..55680970hg38UCSC Ensembl
Innerchr11:55370325..55448446hg19UCSC Ensembl
Innerchr11:55126901..55205022hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3878122
hg1978122
hg1878122
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1909n54
Supporting Variantsnssv775938
Samples
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554871
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