A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2016n71



Internal ID6319636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105238701..105366499hg19UCSC Ensembl
chr14:104309746..104437544hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv902413, nsv902412
SamplesSP54988, MS10311
Known GenesAKT1, KIAA0284, MGC23270, ZBTB42
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv2016n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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