A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469899



Internal ID22527789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3054919..3072614hg38UCSC Ensembl
chr16:3104920..3122615hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3817696
hg1917696
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5879005
Supporting Variants
Samples
Known GenesIL32, MMP25
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469899
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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