A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024226



Internal ID83888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67837000..67843387hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg386388
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141414
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024226
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.01606


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