A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554858



Internal ID15995581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55602150..55685196hg38UCSC Ensembl
Innerchr11:55369626..55452672hg19UCSC Ensembl
Innerchr11:55126202..55209248hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3883047
hg1983047
hg1883047
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1909n54
Supporting Variantsnssv775720, nssv775718, nssv775719
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)nsv554858
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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