A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12979n54



Internal ID22780874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135247660..135422409hg38UCSC Ensembl
chr9:138139506..138314255hg19UCSC Ensembl
chr9:137279327..137454076hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38174750
hg19174750
hg18174750
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615858, nsv615851, nsv615856, nsv615846, nsv615860, nsv615852, nsv615859, nsv615855, nsv615847, nsv615854, nsv615857, nsv615848, nsv615850, nsv615861, nsv615853
Samples1780854090_A, 1782681087_A, 1780862066_A, 1798860567_A, 1780854017_A
Known GenesC9orf62
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12979n54
Frequency
Sample Size17421
Observed Gain21
Observed Loss0
Observed Complex0
Frequencyn/a


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