A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1616n54



Internal ID22769511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5754500..5788000hg38UCSC Ensembl
chr11:5775730..5809230hg19UCSC Ensembl
chr11:5732306..5765806hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3833501
hg1933501
hg1833501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553306, nsv553307, nsv553311, nsv553308, nsv553309
Samples
Known GenesOR52N1, OR52N4, OR52N5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1616n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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