A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17727453



Internal ID151119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12517000..12524000hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg387001
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5431837
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17727453
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.499474


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