A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555079



Internal ID16342488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55915319..55960805hg38UCSC Ensembl
Innerchr11:55682795..55728281hg19UCSC Ensembl
Innerchr11:55439371..55484857hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3845487
hg1945487
hg1845487
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1944n54
Supporting Variantsnssv776846
Samples
Known GenesOR5I1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555079
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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