A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16953444



Internal ID36318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102569823..102569874hg38UCSC Ensembl
chr4:103490980..103491031hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5395570
Supporting Variants
Samples
Known GenesNFKB1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16953444
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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