A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5439085



Internal ID217631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16228659..16232818hg38UCSC Ensembl
chr3:16270166..16274325hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg384160
hg194160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16929185
Samples
Known GenesGALNT15
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5439085
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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