A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16929634



Internal ID20484
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 StatusS
Merged Variantsnsv5435055
Supporting Variants
Samples
Known GenesSUMF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16929634
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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