A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5701n71



Internal ID6323321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121691899..121747335hg19UCSC Ensembl
chr4:121911349..121966785hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv879856, nsv879858, nsv879857, nsv879855
SamplesSP56004, SP54409, SP57418, SP55655, SP54792
Known GenesPRDM5
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv5701n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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