A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3399589



Internal ID15246552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20476085..20482183hg38UCSC Ensembl
Innerchr15:20477085..20481183hg38UCSC Ensembl
Outerchr15:20475085..20483183hg38UCSC Ensembl
chr15:20681338..20687436hg19UCSC Ensembl
Innerchr15:20682338..20686436hg19UCSC Ensembl
Outerchr15:20680338..20688436hg19UCSC Ensembl
chr15:18941352..18947450hg18UCSC Ensembl
Innerchr15:18942352..18946450hg18UCSC Ensembl
Outerchr15:18940352..18948450hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg386099
hg196099
hg186099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8689565
SamplesNA19238
Known GenesHERC2P3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3399589
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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