A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv452n145



Internal ID22813468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:70111585..70243617hg38UCSC Ensembl
chr16:70145488..70277520hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38132033
hg19132033
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3112996, nsv3111407
Samplessample404, sample309
Known GenesCLEC18C, LOC100506060, PDPR
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv452n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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