A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666728



Internal ID9932833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:53974287..54001588hg38UCSC Ensembl
Outerchr3:53974250..54001638hg38UCSC Ensembl
Innerchr3:54008314..54035615hg19UCSC Ensembl
Outerchr3:54008277..54035665hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3827389
hg1927389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5881217
SamplesNA12283
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666728
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