A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17635983



Internal ID21828030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84947701..84948263hg38UCSC Ensembl
chr16:84981307..84981869hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38563
hg19563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028325
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17635983
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