A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12866n54



Internal ID22780761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124275517..124355067hg38UCSC Ensembl
chr9:127037796..127117346hg19UCSC Ensembl
chr9:126077617..126157167hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3879551
hg1979551
hg1879551
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615289, nsv615288
Samples
Known GenesLOC100129034, NEK6, PSMB7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12866n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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