A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5184n54



Internal ID22773079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:70159293..70162848hg38UCSC Ensembl
chr16:70193196..70196751hg19UCSC Ensembl
chr16:68750697..68754252hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg383556
hg193556
hg183556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv572942, nsv572937, nsv572941, nsv572939
Samples
Known GenesPDPR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5184n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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