A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16955985



Internal ID37966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147303905..147304094hg38UCSC Ensembl
chr4:148225057..148225246hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5468218
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16955985
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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