A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8696963



Internal ID13732267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62350755..62353553hg38UCSC Ensembl
Innerchr9:62351755..62352553hg38UCSC Ensembl
Outerchr9:62349755..62354553hg38UCSC Ensembl
chr9:46662056..46664854hg19UCSC Ensembl
Innerchr9:46663056..46663854hg19UCSC Ensembl
Outerchr9:46661056..46665854hg19UCSC Ensembl
chr9:46502052..46504850hg18UCSC Ensembl
Innerchr9:46503052..46503850hg18UCSC Ensembl
Outerchr9:46501052..46505850hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg382799
hg192799
hg182799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3448488
Supporting Variants
SamplesNA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8696963
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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