A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666688



Internal ID9932793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114959879..114971110hg38UCSC Ensembl
chr10:116719638..116730869hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3811232
hg1911232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6248989, essv5618179
SamplesHG00524, HG00512
Known GenesTRUB1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666688
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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