A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16925825



Internal ID17965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:233326724..233327990hg38UCSC Ensembl
chr2:234235370..234236636hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg381267
hg191267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5444766
Supporting Variants
Samples
Known GenesSAG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16925825
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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