A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5425432



Internal ID204395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37100938..37100989hg38UCSC Ensembl
chr19:37591840..37591891hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17723152
Samples
Known GenesZNF420
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5425432
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