A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv437n145



Internal ID22813453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:33752787..34123075hg38UCSC Ensembl
chr16:33555254..33925542hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38370289
hg19370289
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3116933, nsv3116899, nsv3112414, nsv3112862
Samplessample402, sample95, sample419, sample137, sample46
Known GenesRNU6-76P
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv437n145
Frequency
Sample Size467
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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