A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8696984



Internal ID13732282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62465155..62469253hg38UCSC Ensembl
Innerchr9:62466155..62468253hg38UCSC Ensembl
Outerchr9:62464155..62470253hg38UCSC Ensembl
chr9:46776456..46780554hg19UCSC Ensembl
Innerchr9:46777456..46779554hg19UCSC Ensembl
Outerchr9:46775456..46781554hg19UCSC Ensembl
chr9:46616452..46620550hg18UCSC Ensembl
Innerchr9:46617452..46619550hg18UCSC Ensembl
Outerchr9:46615452..46621550hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg384099
hg194099
hg184099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3380804
Supporting Variants
SamplesNA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8696984
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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