A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5472521



Internal ID250227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173935900..173957519hg38UCSC Ensembl
chr4:174857051..174878670hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3821620
hg1921620
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16959308
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5472521
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