A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1527n54



Internal ID22769422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:840477..842775hg38UCSC Ensembl
chr11:840477..842775hg19UCSC Ensembl
chr11:830477..832775hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg382299
hg192299
hg182299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv552886, nsv552883, nsv552884, nsv552885
Samples
Known GenesPOLR2L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1527n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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