A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940129



Internal ID27464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158744307..158753330hg38UCSC Ensembl
chr3:158462096..158471119hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg389024
hg199024
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557394
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940129
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.004059


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