A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16164047



Internal ID2827248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24822050..24822770hg38UCSC Ensembl
Innerchr20:24822059..24822761hg38UCSC Ensembl
Outerchr20:24822041..24822779hg38UCSC Ensembl
chr20:24802686..24803406hg19UCSC Ensembl
Innerchr20:24802695..24803397hg19UCSC Ensembl
Outerchr20:24802677..24803415hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38721
hg19721
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645564
Supporting Variants
SamplesHG02494
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16164047
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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