A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552883



Internal ID16340292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:840477..842627hg38UCSC Ensembl
Innerchr11:840477..842627hg19UCSC Ensembl
Innerchr11:830477..832627hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg382151
hg192151
hg182151
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1527n54
Supporting Variantsnssv763579, nssv763580
Samples
Known GenesPOLR2L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552883
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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