A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5105n54



Internal ID22773000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:46404173..46466539hg38UCSC Ensembl
chr16:46438085..46500451hg19UCSC Ensembl
chr16:44995586..45057952hg18UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg3862367
hg1962367
hg1862367
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv572513, nsv572481, nsv572508, nsv572486, nsv572497, nsv572492, nsv572498, nsv572515, nsv572493, nsv572490, nsv572476, nsv572507, nsv572517, nsv572484, nsv572516, nsv572510, nsv572506, nsv572514, nsv572489, nsv572511, nsv572509, nsv572503, nsv572502, nsv572512
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5105n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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