A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616586



Internal ID7003472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:20940836..20946213hg38UCSC Ensembl
Innerchr8:20940843..20946207hg38UCSC Ensembl
Outerchr8:20940830..20946220hg38UCSC Ensembl
chr8:20798347..20803724hg19UCSC Ensembl
Innerchr8:20798354..20803718hg19UCSC Ensembl
Outerchr8:20798341..20803731hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg385378
hg195378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13132791
SamplesHG01029
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616586
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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