A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259462



Internal ID20468680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155298034..155298034hg38UCSC Ensembl
chr3:155015823..155015823hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767355
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259462
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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