A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1995n71



Internal ID6319615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104143385..104211180hg19UCSC Ensembl
chr14:103213138..103280933hg18UCSC 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 Variantsnsv902309, nsv902310, nsv902312, nsv902311
SamplesIS33684, IS33248, IS33797, IS33455, IS41410, MS10311, IS32322, IS33162
Known GenesKLC1, PPP1R13B, XRCC3, ZFYVE21
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv1995n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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