A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17473481



Internal ID22531374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80061824..80064513hg38UCSC Ensembl
chr16:80095721..80098410hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg382690
hg192690
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5870503
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17473481
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