A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5553092



Internal ID326373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16309521..16309521hg38UCSC Ensembl
chr3:16351028..16351028hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16929192
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5553092
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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