A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3883n71



Internal ID6321503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:42357455..42542999hg19UCSC Ensembl
chr19:47049295..47234839hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv911777, nsv911780, nsv911781
SamplesMS17208, MS18276, MS10698
Known GenesARHGEF1, ATP1A3, CD79A, GRIK5, RABAC1, RPS19
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv3883n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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