A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280816



Internal ID20490034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32211612..32211612hg38UCSC Ensembl
chr5:32211718..32211718hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38751
hg19751
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4768273
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280816
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