A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12926n54



Internal ID20146350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133071778..133080439hg38UCSC Ensembl
chr9:135947165..135955826hg19UCSC Ensembl
chr9:134936986..134945647hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg388662
hg198662
hg188662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615600, nsv615602
Samples
Known GenesCEL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12926n54
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