A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5183n54



Internal ID22773078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:70159293..70162281hg38UCSC Ensembl
chr16:70193196..70196184hg19UCSC Ensembl
chr16:68750697..68753685hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg382989
hg192989
hg182989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv572936, nsv572938, nsv572940
Samples
Known GenesPDPR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5183n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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