A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1608n54



Internal ID22769503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5738230..5740096hg38UCSC Ensembl
chr11:5759460..5761326hg19UCSC Ensembl
chr11:5716036..5717902hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381867
hg191867
hg181867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553279, nsv553278
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1608n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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