A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17098604



Internal ID21475472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69072083..69072083hg38UCSC Ensembl
chr16:69105986..69105986hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5647931
Supporting Variants
SamplesHG03371
Known GenesTANGO6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17098604
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