A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660848



Internal ID9926953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8978927..8979576hg38UCSC Ensembl
chr8:8836437..8837086hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5411978
SamplesNA19920
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660848
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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