A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733862



Internal ID157528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9166181..9166199hg38UCSC Ensembl
chr21:10005014..10005032hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5550209
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733862
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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