A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17726496



Internal ID150162
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 StatusS
Merged Variantsnsv5538079
Supporting Variants
Samples
Known GenesLTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17726496
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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