A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5994528



Internal ID21903871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9822727..9822785hg38UCSC Ensembl
chr3:9864411..9864469hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17523752
Samples
Known GenesARPC4-TTLL3, TTLL3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5994528
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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