A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3361836



Internal ID14862097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16064365..16064479hg38UCSC Ensembl
Innerchr11:16064387..16064455hg38UCSC Ensembl
Outerchr11:16064275..16064569hg38UCSC Ensembl
chr11:16085911..16086025hg19UCSC Ensembl
Innerchr11:16085933..16086001hg19UCSC Ensembl
Outerchr11:16085821..16086115hg19UCSC Ensembl
chr11:16042487..16042601hg18UCSC Ensembl
Innerchr11:16042577..16042509hg18UCSC Ensembl
Outerchr11:16042397..16042691hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38284
hg19284
hg18284
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8672012
SamplesNA19238
Known GenesSOX6
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3361836
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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