A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12609n54



Internal ID22780504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:24645078..24731625hg38UCSC Ensembl
chr9:24645076..24731623hg19UCSC Ensembl
chr9:24635076..24721623hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3886548
hg1986548
hg1886548
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613883, nsv613884
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12609n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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