A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5443268



Internal ID221669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122370457..122376139hg38UCSC Ensembl
chr3:122089304..122094986hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg385683
hg195683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16939483
Samples
Known GenesCCDC58
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5443268
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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