A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937273



Internal ID25565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86490332..86490418hg38UCSC Ensembl
chr3:86539482..86539568hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5433927
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937273
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001873


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