A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv309n145



Internal ID22813325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90886472..90887637hg38UCSC Ensembl
chr13:91538726..91539891hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg381166
hg191166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3113236, nsv3112485
Samplessample361, sample129, sample79, sample292
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv309n145
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