A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5439021



Internal ID217569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154028749..154030076hg38UCSC Ensembl
chr3:153746538..153747865hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg381328
hg191328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17734984
Samples
Known GenesARHGEF26-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5439021
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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