A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12566n54



Internal ID22780461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:12300716..12483221hg38UCSC Ensembl
chr9:12300716..12483221hg19UCSC Ensembl
chr9:12290716..12473221hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38182506
hg19182506
hg18182506
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613605, nsv613602
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12566n54
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