A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554904



Internal ID15995627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55603545..55702527hg38UCSC Ensembl
Innerchr11:55371021..55470003hg19UCSC Ensembl
Innerchr11:55127597..55226579hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3898983
hg1998983
hg1898983
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1908n54
Supporting Variantsnssv776516
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)nsv554904
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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