A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5333n54



Internal ID20138757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89852186..89852908hg38UCSC Ensembl
chr16:89918594..89919316hg19UCSC Ensembl
chr16:88446095..88446817hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38723
hg19723
hg18723
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573796, nsv573797, nsv573801, nsv573794, nsv573803
Samples
Known GenesSPIRE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5333n54
Frequency
Sample Size17421
Observed Gain48
Observed Loss25
Observed Complex0
Frequencyn/a


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