A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669609



Internal ID9935714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:35874786..35874932hg38UCSC Ensembl
chr8:35732304..35732450hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5485154, essv5953849, essv6427318, essv5966317, essv6462788, essv6187145, essv5884062
SamplesNA18508, NA19396, NA19384, NA19403, NA19390, NA19428, NA18501
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669609
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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