A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553238



Internal ID16340647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5361785..5362700hg38UCSC Ensembl
Innerchr11:5383015..5383930hg19UCSC Ensembl
Innerchr11:5339591..5340506hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38916
hg19916
hg18916
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1599n54
Supporting Variantsnssv765364
Samples
Known GenesOR51B5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553238
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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