A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689758



Internal ID15054818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28663065..28664263hg38UCSC Ensembl
Innerchr15:28663263..28664065hg38UCSC Ensembl
Outerchr15:28662065..28665263hg38UCSC Ensembl
chr15:28908211..28909409hg19UCSC Ensembl
Innerchr15:28908409..28909211hg19UCSC Ensembl
Outerchr15:28907211..28910409hg19UCSC Ensembl
chr15:26707252..26708450hg18UCSC Ensembl
Innerchr15:26708252..26707450hg18UCSC Ensembl
Outerchr15:26706252..26709450hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg381199
hg191199
hg181199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3386648
Supporting Variants
SamplesNA19239
Known GenesHERC2P9
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689758
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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