A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3841n71



Internal ID6321461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33682991..33802542hg19UCSC Ensembl
chr19:38374831..38494382hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv911585, nsv911584, nsv911589
SamplesMS10123, MS10311, IS33504
Known GenesCEBPA, LOC80054, LRP3, SLC7A10
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv3841n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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