A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114770



Internal ID21298036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83685844..83693686hg38UCSC Ensembl
Innerchr16:83719449..83727291hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg387843
hg197843
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098250, nssv14098341
Samplessample69, sample26
Known GenesCDH13
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114770
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