A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17710242



Internal ID133908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84835279..84939497hg38UCSC Ensembl
chr16:84868885..84973103hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38104219
hg19104219
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528276
Supporting Variants
Samples
Known GenesCRISPLD2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17710242
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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