A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12621n54



Internal ID22780516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27845762..27897126hg38UCSC Ensembl
chr9:27845760..27897124hg19UCSC Ensembl
chr9:27835760..27887124hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3851365
hg1951365
hg1851365
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613951, nsv613952
SamplesHGDP00846, HGDP00843
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12621n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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