A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8696755



Internal ID13658683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65206853..65216147hg38UCSC Ensembl
Innerchr9:65207836..65215147hg38UCSC Ensembl
Outerchr9:65205832..65217147hg38UCSC Ensembl
chr9:42786456..42795454hg19UCSC Ensembl
Innerchr9:42787456..42794454hg19UCSC Ensembl
Outerchr9:42785456..42796454hg19UCSC Ensembl
chr9:42776452..42785450hg18UCSC Ensembl
Innerchr9:42777452..42784450hg18UCSC Ensembl
Outerchr9:42775452..42786450hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg389295
hg198999
hg188999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3417656
Supporting Variants
SamplesNA12878
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8696755
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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