A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3694n71



Internal ID6321314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5649605..5851336hg19UCSC Ensembl
chr19:5600605..5802336hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv910895, nsv910896
SamplesMS16153, MS18276, MS10769
Known GenesC19orf70, DUS3L, FUT3, FUT6, HSD11B1L, LONP1, NRTN, PRR22, RPL36, SAFB, TMEM146
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv3694n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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