A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3952n71



Internal ID6321572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45821183..45830947hg19UCSC Ensembl
chr19:50513023..50522787hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv912152, nsv912153
SamplesSP54650, SP54442, SP54381, SP54620, SP54448
Known GenesCKM
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv3952n71
Frequency
Sample Size6533
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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