A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665846



Internal ID9585265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25210705..25221834hg38UCSC Ensembl
Outerchr8:25210548..25221987hg38UCSC Ensembl
Innerchr8:25068221..25079350hg19UCSC Ensembl
Outerchr8:25068064..25079503hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3811440
hg1911440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5796952
SamplesNA19213
Known GenesDOCK5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665846
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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