A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3368350



Internal ID15215326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20445385..20455283hg38UCSC Ensembl
Innerchr15:20446385..20454283hg38UCSC Ensembl
Outerchr15:20444385..20456283hg38UCSC Ensembl
chr15:20650638..20660536hg19UCSC Ensembl
Innerchr15:20651638..20659536hg19UCSC Ensembl
Outerchr15:20649638..20661536hg19UCSC Ensembl
chr15:18910652..18920550hg18UCSC Ensembl
Innerchr15:18911652..18919550hg18UCSC Ensembl
Outerchr15:18909652..18921550hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg389899
hg199899
hg189899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8689557
SamplesNA19238
Known GenesHERC2P3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3368350
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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