A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5337n54



Internal ID20138761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89907389..89908560hg38UCSC Ensembl
chr16:89973797..89974968hg19UCSC Ensembl
chr16:88501298..88502469hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381172
hg191172
hg181172
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573830, nsv573817, nsv573824, nsv573834, nsv573823, nsv573821, nsv573822
Samples
Known GenesTCF25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5337n54
Frequency
Sample Size17421
Observed Gain226
Observed Loss38
Observed Complex0
Frequencyn/a


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