A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8178n54



Internal ID20141602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4051238..4107492hg38UCSC Ensembl
chr3:4092922..4149176hg19UCSC Ensembl
chr3:4067922..4124176hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3856255
hg1956255
hg1856255
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv589422, nsv589423
Samples1780854016_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8178n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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