A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645458



Internal ID7032208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19748443..19749247hg38UCSC Ensembl
Innerchr20:19748464..19749226hg38UCSC Ensembl
Outerchr20:19748422..19749268hg38UCSC Ensembl
chr20:19729087..19729891hg19UCSC Ensembl
Innerchr20:19729108..19729870hg19UCSC Ensembl
Outerchr20:19729066..19729912hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38805
hg19805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16155132, essv16155131
SamplesHG00265, NA20763
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645458
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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