A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5339n54



Internal ID20138763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89907596..89908507hg38UCSC Ensembl
chr16:89974004..89974915hg19UCSC Ensembl
chr16:88501505..88502416hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38912
hg19912
hg18912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573833, nsv573836, nsv573835, nsv573827
Samples
Known GenesTCF25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5339n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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