A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662990



Internal ID9929095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9501171..9504831hg38UCSC Ensembl
chr8:9358681..9362341hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg383661
hg193661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5932418
SamplesHG00310
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662990
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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