A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552879



Internal ID16340288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:836864..842627hg38UCSC Ensembl
Innerchr11:836864..842627hg19UCSC Ensembl
Innerchr11:826864..832627hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg385764
hg195764
hg185764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv763574
Samples
Known GenesCD151, POLR2L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552879
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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