A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678959



Internal ID9945064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27795957..27802008hg38UCSC Ensembl
chr3:27837448..27843499hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg386052
hg196052
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5647508
SamplesNA19383
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678959
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