A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5810569



Internal ID8787972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102558704..102560293hg38UCSC Ensembl
chr8:103570932..103572521hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg381590
hg191590
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669040
Supporting Variants
SamplesNA18489
Known GenesODF1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5810569
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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