A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3928058



Internal ID21348128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69361931..69361931hg38UCSC Ensembl
chr16:69395834..69395834hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15183502
SamplesHG002
Known GenesTERF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3928058
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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