A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554487



Internal ID16341896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54684278..54771612hg38UCSC Ensembl
Innerchr11:51347668..51435002hg19UCSC Ensembl
Innerchr11:51204244..51291578hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg3887335
hg1987335
hg1887335
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv774221
Samples
Known GenesOR4A5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554487
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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