A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12902n54



Internal ID22780797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129453159..129471535hg38UCSC Ensembl
chr9:132215438..132233814hg19UCSC Ensembl
chr9:131255259..131273635hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3818377
hg1918377
hg1818377
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615464, nsv615465, nsv615454, nsv615466
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12902n54
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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