A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv289n145



Internal ID22813305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44834707..44852396hg38UCSC Ensembl
chr13:45408843..45426532hg19UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg3817690
hg1917690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3117249, nsv3114348
Samplessample282, sample285, sample308, sample410
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv289n145
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer