A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16938923



Internal ID26669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142932107..142932144hg38UCSC Ensembl
chr3:142650949..142650986hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38358
hg19358
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561914
Supporting Variants
Samples
Known GenesLOC100507389
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16938923
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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