A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12478n54



Internal ID22780373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:2689244..2711637hg38UCSC Ensembl
chr9:2689244..2711637hg19UCSC Ensembl
chr9:2679244..2701637hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3822394
hg1922394
hg1822394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613139, nsv613141, nsv613140
SamplesHGDP00469, HGDP00460
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12478n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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