A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554906



Internal ID15995629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55603545..55722901hg38UCSC Ensembl
Innerchr11:55371021..55490377hg19UCSC Ensembl
Innerchr11:55127597..55246953hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38119357
hg19119357
hg18119357
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1908n54
Supporting Variantsnssv1175382
SamplesHGDP01003
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)nsv554906
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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