A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659825



Internal ID9925930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188115125..188131841hg38UCSC Ensembl
chr3:187832913..187849629hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3816717
hg1916717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5422732
SamplesHG00463
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659825
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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