A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661752



Internal ID9581171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:93645492..93647115hg38UCSC Ensembl
Outerchr8:93645455..93647165hg38UCSC Ensembl
Innerchr8:94657720..94659343hg19UCSC Ensembl
Outerchr8:94657683..94659393hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg381711
hg191711
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5570784
SamplesNA18542
Known GenesLINC00535
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661752
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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