A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17020178



Internal ID81086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27194806..27296018hg38UCSC Ensembl
chr9:27194804..27296016hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38101213
hg19101213
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488996
Supporting Variants
Samples
Known GenesEQTN, LINC00032, TEK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17020178
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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