A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16956291



Internal ID38166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:134171656..134183385hg38UCSC Ensembl
chr4:135092811..135104540hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3811730
hg1911730
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558389
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16956291
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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