A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275946



Internal ID20485164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2833326..2833547hg38UCSC Ensembl
chr16:2883327..2883548hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739835
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275946
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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