A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100274



Internal ID22009507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3508912..3508912hg38UCSC Ensembl
chr16:3558912..3558912hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607334
Samples
Known GenesCLUAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100274
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer