A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17603830



Internal ID21795877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2857067..2857250hg38UCSC Ensembl
chr16:2907068..2907251hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6033522
Supporting Variants
Samples
Known GenesPRSS22
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17603830
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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