A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5550775



Internal ID324290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189928071..189928071hg38UCSC Ensembl
chr3:189645860..189645860hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16942715
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5550775
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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