A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5614997



Internal ID8592400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:94626232..94627570hg38UCSC Ensembl
Outerchr8:94626075..94627723hg38UCSC Ensembl
Innerchr8:95638460..95639798hg19UCSC Ensembl
Outerchr8:95638303..95639951hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg381649
hg191649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2660044
Supporting Variants
SamplesNA19316
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5614997
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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