A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3932n54



Internal ID18996108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102776388..102778238hg38UCSC Ensembl
chr14:103242725..103244575hg19UCSC Ensembl
chr14:102312478..102314328hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg381851
hg191851
hg181851
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565953, nsv565952
Samples
Known GenesTRAF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3932n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss3
Observed Complex0
Frequencyn/a


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