A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733768



Internal ID157434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:5256973..5393050hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38136078
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146999
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733768
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.148896


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