A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17706367



Internal ID130033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3491792..3503249hg38UCSC Ensembl
chr16:3541792..3553249hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3811458
hg1911458
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6144827
Supporting Variants
Samples
Known GenesC16orf90, CLUAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17706367
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000937


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