A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5334n54



Internal ID20138758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89852237..89853617hg38UCSC Ensembl
chr16:89918645..89920025hg19UCSC Ensembl
chr16:88446146..88447526hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381381
hg191381
hg181381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573809, nsv573804
Samples
Known GenesSPIRE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5334n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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