A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554809



Internal ID15995532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55592737..55669650hg38UCSC Ensembl
Innerchr11:55360213..55437126hg19UCSC Ensembl
Innerchr11:55116789..55193702hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3876914
hg1976914
hg1876914
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv775169
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)nsv554809
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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