A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5435055



Internal ID213712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4418446..4483446hg38UCSC Ensembl
chr3:4460130..4525130hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3865001
hg1965001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16929634
Samples
Known GenesSUMF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5435055
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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