A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991469



Internal ID21900812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119342724..119353658hg38UCSC Ensembl
chr3:119061571..119072505hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3810935
hg1910935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17540570
Samples
Known GenesARHGAP31
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991469
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