A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16958073



Internal ID39371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:149661983..149671175hg38UCSC Ensembl
chr4:150583135..150592327hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg389193
hg199193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5471357
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16958073
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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