A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16155725



Internal ID5665888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20756251..20760537hg38UCSC Ensembl
Innerchr20:20756251..20760537hg38UCSC Ensembl
Outerchr20:20756051..20760703hg38UCSC Ensembl
chr20:20736894..20741180hg19UCSC Ensembl
Innerchr20:20736894..20741180hg19UCSC Ensembl
Outerchr20:20736694..20741346hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg384287
hg194287
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645484
Supporting Variants
SamplesNA19075
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16155725
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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