A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3933n54



Internal ID20137357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102777002..102778238hg38UCSC Ensembl
chr14:103243339..103244575hg19UCSC Ensembl
chr14:102313092..102314328hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg381237
hg191237
hg181237
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565958, nsv565957, nsv565965, nsv565959, nsv565966, nsv565967, nsv565964, nsv565956, nsv565961, nsv565960
Samples
Known GenesTRAF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3933n54
Frequency
Sample Size17421
Observed Gain36
Observed Loss21
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer