A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645690



Internal ID7032439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33961587..33970304hg38UCSC Ensembl
Innerchr20:33961587..33970304hg38UCSC Ensembl
Outerchr20:33961387..33970457hg38UCSC Ensembl
chr20:32549393..32558110hg19UCSC Ensembl
Innerchr20:32549393..32558110hg19UCSC Ensembl
Outerchr20:32549193..32558263hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg388718
hg198718
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16175883, essv16175881, essv16175882, essv16175880, essv16175884, essv16175879
SamplesHG02614, HG02595, HG03085, HG02557, HG02799, HG02721
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645690
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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