A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12572n54



Internal ID22780467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14590807..14622954hg38UCSC Ensembl
chr9:14590805..14622952hg19UCSC Ensembl
chr9:14580805..14612952hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3832148
hg1932148
hg1832148
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613640, nsv613641
Samples
Known GenesZDHHC21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12572n54
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