A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16957296



Internal ID38845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:135471983..135638834hg38UCSC Ensembl
chr4:136393138..136559989hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38166852
hg19166852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455452
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16957296
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