A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16939134



Internal ID26806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129209278..129215499hg38UCSC Ensembl
chr3:128928121..128934342hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg386222
hg196222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451317
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16939134
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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