A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645692



Internal ID7032441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33964446..33966614hg38UCSC Ensembl
Innerchr20:33964483..33966578hg38UCSC Ensembl
Outerchr20:33964410..33966651hg38UCSC Ensembl
chr20:32552252..32554420hg19UCSC Ensembl
Innerchr20:32552289..32554384hg19UCSC Ensembl
Outerchr20:32552216..32554457hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg382169
hg192169
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16175891, essv16175889, essv16175893, essv16175888, essv16175892, essv16175890
SamplesHG02614, HG02595, HG03085, HG02783, HG02557, HG02799
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645692
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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