A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645494



Internal ID7032243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21412708..21432831hg38UCSC Ensembl
Innerchr20:21412719..21432820hg38UCSC Ensembl
Outerchr20:21412697..21432842hg38UCSC Ensembl
chr20:21393346..21413469hg19UCSC Ensembl
Innerchr20:21393357..21413458hg19UCSC Ensembl
Outerchr20:21393335..21413480hg19UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg3820124
hg1920124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16158026
SamplesHG04186
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645494
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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