A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3432361



Internal ID15279317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62281655..62287553hg38UCSC Ensembl
Innerchr9:62282655..62286553hg38UCSC Ensembl
Outerchr9:62280655..62288553hg38UCSC Ensembl
chr9:46592956..46598854hg19UCSC Ensembl
Innerchr9:46593956..46597854hg19UCSC Ensembl
Outerchr9:46591956..46599854hg19UCSC Ensembl
chr9:46432952..46438850hg18UCSC Ensembl
Innerchr9:46433952..46437850hg18UCSC Ensembl
Outerchr9:46431952..46439850hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg385899
hg195899
hg185899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8696956
SamplesNA12878
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3432361
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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