A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5237n71



Internal ID6322857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:121873433..121903836hg19UCSC Ensembl
chr3:123356123..123386526hg18UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv877388, nsv877386, nsv877385
SamplesSP54043, SP57469, SP55021
Known GenesCASR
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv5237n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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