A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616619



Internal ID7003505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22981916..22983238hg38UCSC Ensembl
Innerchr8:22981916..22983238hg38UCSC Ensembl
Outerchr8:22981659..22983505hg38UCSC Ensembl
chr8:22839429..22840751hg19UCSC Ensembl
Innerchr8:22839429..22840751hg19UCSC Ensembl
Outerchr8:22839172..22841018hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg381323
hg191323
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13134403
SamplesHG03611
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616619
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