A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689699



Internal ID15054630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22500387..22501285hg38UCSC Ensembl
Innerchr15:22500386..22501286hg38UCSC Ensembl
Outerchr15:22499387..22502285hg38UCSC Ensembl
chr15:23371811..23372709hg19UCSC Ensembl
Innerchr15:23371810..23372710hg19UCSC Ensembl
Outerchr15:23370811..23373709hg19UCSC Ensembl
chr15:20923252..20924150hg18UCSC Ensembl
Innerchr15:20924151..20923251hg18UCSC Ensembl
Outerchr15:20922252..20925150hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38899
hg19899
hg18899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3341142
Supporting Variants
SamplesNA19239
Known GenesHERC2P2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689699
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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