A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5239n54



Internal ID22773134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80917409..80955962hg38UCSC Ensembl
chr16:80951306..80989859hg19UCSC Ensembl
chr16:79508807..79547360hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3838554
hg1938554
hg1838554
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573304, nsv573303
SamplesHGDP00994, HGDP01408
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5239n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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