A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733890



Internal ID157556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9953394..9953445hg38UCSC Ensembl
chr21:10431422..10431473hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5419993
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733890
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.004527


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