A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554893



Internal ID15995616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55603545..55662960hg38UCSC Ensembl
Innerchr11:55371021..55430436hg19UCSC Ensembl
Innerchr11:55127597..55187012hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3859416
hg1959416
hg1859416
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1914n54
Supporting Variantsnssv776007
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)nsv554893
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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