A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689700



Internal ID15095182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22473687..22482285hg38UCSC Ensembl
Innerchr15:22474687..22481285hg38UCSC Ensembl
Outerchr15:22472687..22483285hg38UCSC Ensembl
chr15:23390811..23399409hg19UCSC Ensembl
Innerchr15:23391811..23398409hg19UCSC Ensembl
Outerchr15:23389811..23400409hg19UCSC Ensembl
chr15:20942252..20950850hg18UCSC Ensembl
Innerchr15:20943252..20949850hg18UCSC Ensembl
Outerchr15:20941252..20951850hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg388599
hg198599
hg188599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3335466
Supporting Variants
SamplesNA19240
Known GenesHERC2P7
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689700
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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