A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733757



Internal ID157423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:5062000..5069000hg38UCSC Ensembl
chr21:45613033..45621553hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg387001
hg198521
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146277
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733757
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000558


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