A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8696813



Internal ID13731797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64457457..64470667hg38UCSC Ensembl
Innerchr9:64458457..64469666hg38UCSC Ensembl
Outerchr9:64456460..64471693hg38UCSC Ensembl
chr9:43026256..43039454hg19UCSC Ensembl
Innerchr9:43027256..43038454hg19UCSC Ensembl
Outerchr9:43025256..43040454hg19UCSC Ensembl
chr9:43016252..43029450hg18UCSC Ensembl
Innerchr9:43017252..43028450hg18UCSC Ensembl
Outerchr9:43015252..43030450hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3813211
hg1913199
hg1813199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3353453
Supporting Variants
SamplesNA12892
Known GenesFAM95B1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8696813
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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