A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1820n54



Internal ID22769715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:50504005..50800919hg38UCSC Ensembl
chr11:50463176..50760090hg19UCSC Ensembl
chr11:50419752..50716666hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38296915
hg19296915
hg18296915
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv554418, nsv554417
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1820n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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