A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668490



Internal ID9934595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28381287..28388771hg38UCSC Ensembl
chr8:28238804..28246288hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg387485
hg197485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5750266
SamplesNA19661
Known GenesZNF395
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668490
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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