A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8740833



Internal ID15084168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98007026..98007111hg38UCSC Ensembl
Innerchr15:98007061..98007076hg38UCSC Ensembl
Outerchr15:98006987..98007161hg38UCSC Ensembl
chr15:98550256..98550341hg19UCSC Ensembl
Innerchr15:98550291..98550306hg19UCSC Ensembl
Outerchr15:98550217..98550391hg19UCSC Ensembl
chr15:96367719..96367804hg18UCSC Ensembl
Innerchr15:96367769..96367754hg18UCSC Ensembl
Outerchr15:96367669..96367854hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3886
hg1986
hg1886
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3380544
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8740833
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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