A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554803



Internal ID15995526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55572903..55641224hg38UCSC Ensembl
Innerchr11:55340379..55408700hg19UCSC Ensembl
Innerchr11:55096955..55165276hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3868322
hg1968322
hg1868322
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv775163
Samples
Known GenesOR4C11, OR4C16, OR4P4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554803
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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