A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554892



Internal ID15995615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55603545..55656731hg38UCSC Ensembl
Innerchr11:55371021..55424207hg19UCSC Ensembl
Innerchr11:55127597..55180783hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3853187
hg1953187
hg1853187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1914n54
Supporting Variantsnssv776003, nssv776004, nssv776005, nssv776006
Samples
Known GenesOR4C11, OR4P4, OR4S2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554892
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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