A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12551n54



Internal ID22780446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11969789..12416645hg38UCSC Ensembl
chr9:11969789..12416645hg19UCSC Ensembl
chr9:11959789..12406645hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38446857
hg19446857
hg18446857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613546, nsv613519
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12551n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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