A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5263n54



Internal ID20138687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84403617..84435705hg38UCSC Ensembl
chr16:84437223..84469311hg19UCSC Ensembl
chr16:82994724..83026812hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3832089
hg1932089
hg1832089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573432, nsv573433, nsv573431
Samples
Known GenesATP2C2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5263n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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