A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16944857



Internal ID30572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187745250..187745261hg38UCSC Ensembl
chr3:187463038..187463049hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5538404
Supporting Variants
Samples
Known GenesBCL6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16944857
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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