A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5542184



Internal ID316628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6738469..6738505hg38UCSC Ensembl
chr4:6740196..6740232hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16945814
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5542184
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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