A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902289



Internal ID22677445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87012339..87032627hg38UCSC Ensembl
chr4:87933491..87953779hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3820289
hg1920289
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421494
Samples
Known GenesAFF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902289
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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