A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16166519



Internal ID5841374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25699120..25701250hg38UCSC Ensembl
Innerchr20:25699122..25701248hg38UCSC Ensembl
Outerchr20:25699118..25701252hg38UCSC Ensembl
chr20:25679756..25681886hg19UCSC Ensembl
Innerchr20:25679758..25681884hg19UCSC Ensembl
Outerchr20:25679754..25681888hg19UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg382131
hg192131
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645591
Supporting Variants
SamplesNA19213
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16166519
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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