A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2368n71



Internal ID6319988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43257475..43482127hg19UCSC Ensembl
chr15:41044767..41269419hg18UCSC 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 Variantsnsv904144, nsv904136, nsv904139
SamplesIS33797, IS33616, IS31187, IS37065
Known GenesCCNDBP1, TMEM62, UBR1
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv2368n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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