A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552981



Internal ID15993704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1362059..1412191hg38UCSC Ensembl
Innerchr11:1383289..1433421hg19UCSC Ensembl
Innerchr11:1339865..1389997hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3850133
hg1950133
hg1850133
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv764277
Samples
Known GenesBRSK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552981
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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