A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8625n54



Internal ID20142049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142093917..142265796hg38UCSC Ensembl
chr3:141812759..141984638hg19UCSC Ensembl
chr3:143295449..143467328hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38171880
hg19171880
hg18171880
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv591913, nsv591911
Samples
Known GenesGK5, TFDP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8625n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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