A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689561



Internal ID15053962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20455785..20464383hg38UCSC Ensembl
Innerchr15:20456785..20463383hg38UCSC Ensembl
Outerchr15:20454785..20465383hg38UCSC Ensembl
chr15:20661038..20669636hg19UCSC Ensembl
Innerchr15:20662038..20668636hg19UCSC Ensembl
Outerchr15:20660038..20670636hg19UCSC Ensembl
chr15:18921052..18929650hg18UCSC Ensembl
Innerchr15:18922052..18928650hg18UCSC Ensembl
Outerchr15:18920052..18930650hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg388599
hg198599
hg188599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3419194
Supporting Variants
SamplesNA19239
Known GenesHERC2P3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689561
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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