A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12884n54



Internal ID20146308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128688840..128690393hg38UCSC Ensembl
chr9:131451119..131452672hg19UCSC Ensembl
chr9:130490940..130492493hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381554
hg191554
hg181554
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615402, nsv615396, nsv615397, nsv615398, nsv615399
Samples
Known GenesSET
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12884n54
Frequency
Sample Size17421
Observed Gain18
Observed Loss0
Observed Complex0
Frequencyn/a


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