A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13267372



Internal ID3269188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98344727..98347345hg38UCSC Ensembl
Innerchr8:98344782..98347291hg38UCSC Ensembl
Outerchr8:98344673..98347400hg38UCSC Ensembl
chr8:99356955..99359573hg19UCSC Ensembl
Innerchr8:99357010..99359519hg19UCSC Ensembl
Outerchr8:99356901..99359628hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg382619
hg192619
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3618150
Supporting Variants
SamplesNA19152
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13267372
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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