A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616618



Internal ID6656814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22964260..22966710hg38UCSC Ensembl
Innerchr8:22964301..22966669hg38UCSC Ensembl
Outerchr8:22964219..22966751hg38UCSC Ensembl
chr8:22821773..22824223hg19UCSC Ensembl
Innerchr8:22821814..22824182hg19UCSC Ensembl
Outerchr8:22821732..22824264hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg382451
hg192451
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13134402
SamplesHG01798
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616618
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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