A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12895n54



Internal ID22780790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129431819..129466284hg38UCSC Ensembl
chr9:132194098..132228563hg19UCSC Ensembl
chr9:131233919..131268384hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3834466
hg1934466
hg1834466
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615435, nsv615438
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12895n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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