A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1565n54



Internal ID20134989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1844330..1891496hg38UCSC Ensembl
chr11:1865560..1912726hg19UCSC Ensembl
chr11:1822136..1869302hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3847167
hg1947167
hg1847167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553057, nsv553056
SamplesHGDP01339
Known GenesLSP1, MIR4298
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1565n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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