A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645511



Internal ID7032260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22927149..22938532hg38UCSC Ensembl
Innerchr20:22927149..22938532hg38UCSC Ensembl
Outerchr20:22926923..22938799hg38UCSC Ensembl
chr20:22907786..22919169hg19UCSC Ensembl
Innerchr20:22907786..22919169hg19UCSC Ensembl
Outerchr20:22907560..22919436hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3811384
hg1911384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16160653
SamplesHG00543
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645511
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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