A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13161446



Internal ID3163262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33374071..33376340hg38UCSC Ensembl
Innerchr8:33374086..33376325hg38UCSC Ensembl
Outerchr8:33374056..33376355hg38UCSC Ensembl
chr8:33231589..33233858hg19UCSC Ensembl
Innerchr8:33231604..33233843hg19UCSC Ensembl
Outerchr8:33231574..33233873hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg382270
hg192270
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3616832
Supporting Variants
SamplesNA20589
Known GenesFUT10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13161446
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer