A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5551950



Internal ID325368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73828190..73828203hg38UCSC Ensembl
chr14:74294893..74294906hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698317
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5551950
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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