A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645189



Internal ID7031940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:9486110..9488304hg38UCSC Ensembl
Innerchr20:9486117..9488298hg38UCSC Ensembl
Outerchr20:9486104..9488311hg38UCSC Ensembl
chr20:9466757..9468951hg19UCSC Ensembl
Innerchr20:9466764..9468945hg19UCSC Ensembl
Outerchr20:9466751..9468958hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg382195
hg192195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16139525
SamplesNA19317
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645189
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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