A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5338n54



Internal ID20138762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89907493..89908286hg38UCSC Ensembl
chr16:89973901..89974694hg19UCSC Ensembl
chr16:88501402..88502195hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38794
hg19794
hg18794
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573826, nsv573819, nsv573818
Samples
Known GenesTCF25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5338n54
Frequency
Sample Size17421
Observed Gain18
Observed Loss5
Observed Complex0
Frequencyn/a


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