A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17080220



Internal ID21448137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:62652710..62652710hg38UCSC Ensembl
chr16:62686614..62686614hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38525
hg19525
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5647069
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17080220
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