A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936288



Internal ID24920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:81959232..81975084hg38UCSC Ensembl
chr3:82008383..82024235hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3815853
hg1915853
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438605
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936288
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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