A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554798



Internal ID15995521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55315958..55388958hg38UCSC Ensembl
Innerchr11:55083434..55156434hg19UCSC Ensembl
Innerchr11:54840010..54913010hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3873001
hg1973001
hg1873001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv775159
Samples
Known GenesOR4A15, OR4A16
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554798
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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