A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666863



Internal ID4711197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:12831631..12837914hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsessv5941181, essv6402998, essv5406319, essv5958051
SamplesNA20510, HG00112, NA19783, HG01187
Known GenesPHACTR1
Method
Analysis
Platform
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666863
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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