A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645744



Internal ID6685805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36820233..36823133hg38UCSC Ensembl
Innerchr20:36820263..36823104hg38UCSC Ensembl
Outerchr20:36820204..36823163hg38UCSC Ensembl
chr20:35448636..35451536hg19UCSC Ensembl
Innerchr20:35448666..35451507hg19UCSC Ensembl
Outerchr20:35448607..35451566hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg382901
hg192901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16179859
SamplesNA21120
Known GenesSOGA1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645744
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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