A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666331



Internal ID9932436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:71651449..71654263hg38UCSC Ensembl
Outerchr8:71651412..71654313hg38UCSC Ensembl
Innerchr8:72563684..72566498hg19UCSC Ensembl
Outerchr8:72563647..72566548hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg382902
hg192902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6466032
SamplesNA18536
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666331
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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