A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669038



Internal ID9935143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:139111723..139114810hg38UCSC Ensembl
Outerchr8:139111686..139114860hg38UCSC Ensembl
Innerchr8:140123966..140127053hg19UCSC Ensembl
Outerchr8:140123929..140127103hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg383175
hg193175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6441610
SamplesNA20790
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669038
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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