A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936584



Internal ID25111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:121668277..121669196hg38UCSC Ensembl
chr3:121387124..121388043hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38920
hg19920
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562213
Supporting Variants
Samples
Known GenesGOLGB1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936584
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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