A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8688149



Internal ID13692268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89037015..89042513hg38UCSC Ensembl
Innerchr10:89038015..89041513hg38UCSC Ensembl
Outerchr10:89036015..89043513hg38UCSC Ensembl
chr10:90796772..90802270hg19UCSC Ensembl
Innerchr10:90797772..90801270hg19UCSC Ensembl
Outerchr10:90795772..90803270hg19UCSC Ensembl
chr10:90786752..90792250hg18UCSC Ensembl
Innerchr10:90787752..90791250hg18UCSC Ensembl
Outerchr10:90785752..90793250hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg385499
hg195499
hg185499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3335977
Supporting Variants
SamplesNA12891
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8688149
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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