A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689682



Internal ID15020559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22532087..22552185hg38UCSC Ensembl
Innerchr15:22533087..22551185hg38UCSC Ensembl
Outerchr15:22531087..22553185hg38UCSC Ensembl
chr15:23320911..23341009hg19UCSC Ensembl
Innerchr15:23321911..23340009hg19UCSC Ensembl
Outerchr15:23319911..23342009hg19UCSC Ensembl
chr15:20872352..20892450hg18UCSC Ensembl
Innerchr15:20873352..20891450hg18UCSC Ensembl
Outerchr15:20871352..20893450hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3820099
hg1920099
hg1820099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3429800
Supporting Variants
SamplesNA19238
Known GenesHERC2P2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689682
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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