A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12651n54



Internal ID22780546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:30677335..30822801hg38UCSC Ensembl
chr9:30677333..30822799hg19UCSC Ensembl
chr9:30667333..30812799hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38145467
hg19145467
hg18145467
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv614111, nsv614112
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12651n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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