A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8306n54



Internal ID22776201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46755146..46789244hg38UCSC Ensembl
chr3:46796636..46830734hg19UCSC Ensembl
chr3:46771640..46805738hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3834099
hg1934099
hg1834099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv590198, nsv590187
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8306n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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