A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675732



Internal ID9941837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85974902..85980766hg38UCSC Ensembl
chr16:86008508..86014372hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg385865
hg195865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5945951
SamplesHG00151
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675732
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer