A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16179859



Internal ID6181675
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645744
Supporting Variants
SamplesNA21120
Known GenesSOGA1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16179859
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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