A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17727376



Internal ID151043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11332000..11337400hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg385401
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416269
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17727376
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.5


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