A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5336n54



Internal ID20138760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89907389..89908507hg38UCSC Ensembl
chr16:89973797..89974915hg19UCSC Ensembl
chr16:88501298..88502416hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381119
hg191119
hg181119
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573829, nsv573814, nsv573828, nsv573820, nsv573815
Samples
Known GenesTCF25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5336n54
Frequency
Sample Size17421
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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