A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677828



Internal ID4722162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17094429..17101637hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsessv6378633, essv5499165, essv6354440, essv6321886, essv5550825
SamplesNA12043, HG00736, NA11995, HG01073, HG00262
Known GenesCUBN
Method
Analysis
Platform
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677828
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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