A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17020230



Internal ID81122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27766900..27817944hg38UCSC Ensembl
chr9:27766898..27817942hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3851045
hg1951045
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484352
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17020230
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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