A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1982n71



Internal ID6319602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101251989..101313093hg19UCSC Ensembl
chr14:100321742..100382846hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv902238, nsv902239
SamplesMS10311, IS32322, IS39233
Known GenesMEG3, MIR2392
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv1982n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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