A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16938730



Internal ID26549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120464539..120473619hg38UCSC Ensembl
chr3:120183386..120192466hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg389081
hg199081
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563762
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16938730
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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