A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677822



Internal ID4722156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:121959730..121963194hg19UCSC Ensembl
Outerchr3:121959573..121963347hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsessv5936992
SamplesNA19835
Known GenesCASR
Method
Analysis
Platform
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677822
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