A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5448840



Internal ID227097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167725736..167725811hg38UCSC Ensembl
chr3:167443524..167443599hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16941259
Samples
Known GenesPDCD10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5448840
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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