A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16939136



Internal ID26807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129213049..129213085hg38UCSC Ensembl
chr3:128931892..128931928hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5539071
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16939136
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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