A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672596



Internal ID9938701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:15865999..15895063hg38UCSC Ensembl
chr8:15723508..15752572hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3829065
hg1929065
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5628595
SamplesNA18541
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672596
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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