A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3367594



Internal ID15214570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25871654..25871794hg38UCSC Ensembl
Innerchr15:25871704..25871744hg38UCSC Ensembl
Outerchr15:25871604..25871844hg38UCSC Ensembl
chr15:26116801..26116941hg19UCSC Ensembl
Innerchr15:26116851..26116891hg19UCSC Ensembl
Outerchr15:26116751..26116991hg19UCSC Ensembl
chr15:23667894..23668034hg18UCSC Ensembl
Innerchr15:23667944..23667984hg18UCSC Ensembl
Outerchr15:23667844..23668084hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38141
hg19141
hg18141
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8740815
SamplesNA12878
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3367594
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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