A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616160



Internal ID6656357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8931296..8937995hg38UCSC Ensembl
Innerchr8:8931796..8937495hg38UCSC Ensembl
Outerchr8:8930296..8938995hg38UCSC Ensembl
chr8:8788806..8795505hg19UCSC Ensembl
Innerchr8:8789306..8795005hg19UCSC Ensembl
Outerchr8:8787806..8796505hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg386700
hg196700
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13093745, essv13093746
SamplesNA20761, HG02798
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616160
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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