A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669589



Internal ID9935694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38010449..38014958hg38UCSC Ensembl
chr8:37867967..37872476hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg384510
hg194510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6359908
SamplesHG00684
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669589
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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