A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17080976



Internal ID21436900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23853966..23853966hg38UCSC Ensembl
chr16:23865287..23865287hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5659240
Supporting Variants
SamplesHG00731
Known GenesPRKCB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17080976
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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