A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17727769



Internal ID151435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21219932..21278282hg38UCSC Ensembl
chr22:21574221..21632571hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3858351
hg1958351
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146926
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17727769
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002194


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