A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2369n71



Internal ID6319989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43268970..43414673hg19UCSC Ensembl
chr15:41056262..41201965hg18UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv904141, nsv904140, nsv904137, nsv904145, nsv904142, nsv904143
SamplesIS31564, IS40368, IS30923, IS33514, IS30835, IS31179, IS31306, IS35145, IS40067, IS38057
Known GenesUBR1
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv2369n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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