A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3383884



Internal ID15230854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63060855..63061853hg38UCSC Ensembl
Innerchr20:63060854..63061854hg38UCSC Ensembl
Outerchr20:63059855..63062853hg38UCSC Ensembl
chr20:61692207..61693205hg19UCSC Ensembl
Innerchr20:61692206..61693206hg19UCSC Ensembl
Outerchr20:61691207..61694205hg19UCSC Ensembl
chr20:61162652..61163650hg18UCSC Ensembl
Innerchr20:61163651..61162651hg18UCSC Ensembl
Outerchr20:61161652..61164650hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38999
hg19999
hg18999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8692608
SamplesNA19239
Known GenesLOC63930
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3383884
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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