A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5086n54



Internal ID22772981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:35911586..35994041hg38UCSC Ensembl
chr16:35145957..35228412hg19UCSC Ensembl
chr16:35003458..35085913hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg3882456
hg1982456
hg1882456
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv572393, nsv572391
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5086n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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