A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089585



Internal ID21440530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84735964..84735964hg38UCSC Ensembl
chr16:84769570..84769570hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5649630
Supporting Variants
SamplesHG00732
Known GenesUSP10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089585
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