A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885985



Internal ID22660972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2822373..2824897hg38UCSC Ensembl
chr16:2872374..2874898hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382525
hg192525
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469891
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885985
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