A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940918



Internal ID27980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153185667..153185694hg38UCSC Ensembl
chr3:152903456..152903483hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5547649
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940918
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.093544


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