A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12625n54



Internal ID22780520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28188481..28348015hg38UCSC Ensembl
chr9:28188479..28348013hg19UCSC Ensembl
chr9:28178479..28338013hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38159535
hg19159535
hg18159535
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613970, nsv613968, nsv613969, nsv613967, nsv613966
Samples
Known GenesLINGO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12625n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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