A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2991n71



Internal ID6320611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88844932..88921493hg19UCSC Ensembl
chr16:87372433..87448994hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv907323, nsv907328, nsv907327
SamplesIS41634, IS33361, MS10386, IS32803
Known GenesAPRT, CDT1, GALNS, PIEZO1
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv2991n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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