A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5658523



Internal ID21606828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81013242..81013242hg38UCSC Ensembl
chr16:81046847..81046847hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17099403
SamplesHG01505
Known GenesCENPN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5658523
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