A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1802n71



Internal ID6319422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113915485..114109382hg19UCSC Ensembl
chr13:112963486..113157383hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv901069, nsv901070
SamplesMS10311, MS13770
Known GenesADPRHL1, CUL4A, GRTP1, LAMP1
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv1802n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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