A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288029



Internal ID20497247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88561979..88561979hg38UCSC Ensembl
chr16:88628387..88628387hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767287
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288029
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