A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645763



Internal ID7032511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37575316..37576414hg38UCSC Ensembl
Innerchr20:37575380..37576351hg38UCSC Ensembl
Outerchr20:37575253..37576478hg38UCSC Ensembl
chr20:36203718..36204816hg19UCSC Ensembl
Innerchr20:36203782..36204753hg19UCSC Ensembl
Outerchr20:36203655..36204880hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg381099
hg191099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16180217
SamplesHG02147
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645763
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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