A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16956561



Internal ID38350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145832687..145838180hg38UCSC Ensembl
chr4:146753839..146759332hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg385494
hg195494
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5462521
Supporting Variants
Samples
Known GenesZNF827
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16956561
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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