A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554887



Internal ID15995610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55603545..55641188hg38UCSC Ensembl
Innerchr11:55371021..55408664hg19UCSC Ensembl
Innerchr11:55127597..55165240hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3837644
hg1937644
hg1837644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1911n54
Supporting Variantsnssv775980
Samples
Known GenesOR4C11, OR4P4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554887
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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