A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5653816



Internal ID21602121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:22818800..22818800hg38UCSC Ensembl
chr16:22830121..22830121hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38255
hg19255
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086668
SamplesHG00732
Known GenesHS3ST2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5653816
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