A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663138



Internal ID9929243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:108264705..108272353hg38UCSC Ensembl
Outerchr8:108264548..108272506hg38UCSC Ensembl
Innerchr8:109276934..109284582hg19UCSC Ensembl
Outerchr8:109276777..109284735hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg387959
hg197959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5817808, essv5616377
SamplesHG00731, HG00320
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663138
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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