A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5538079



Internal ID313244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:28929393..28929605hg38UCSC Ensembl
chr21:30301715..30301927hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17726496
Samples
Known GenesLTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5538079
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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