A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668450



Internal ID9934555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26707654..26788040hg38UCSC Ensembl
chr9:26707652..26788038hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3880387
hg1980387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6213147, essv5819887, essv5996701
SamplesHG00443, HG00557, HG00707
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668450
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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