A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7865829



Internal ID13318097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80207293..80207301hg38UCSC Ensembl
Innerchr15:80207295..80207299hg38UCSC Ensembl
Outerchr15:80207291..80207303hg38UCSC Ensembl
chr15:80499635..80499643hg19UCSC Ensembl
Innerchr15:80499637..80499641hg19UCSC Ensembl
Outerchr15:80499633..80499645hg19UCSC Ensembl
chr15:78286690..78286698hg18UCSC Ensembl
Innerchr15:78286692..78286696hg18UCSC Ensembl
Outerchr15:78286688..78286700hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3856
hg1956
hg1856
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3350295
Supporting Variants
SamplesNA12005
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7865829
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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