A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17727351



Internal ID151018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:10750000..10759000hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg389001
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5426189
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17727351
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.5


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