A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025432



Internal ID84689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87159176..87159409hg38UCSC Ensembl
chr9:89774091..89774324hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476151
Supporting Variants
Samples
Known GenesC9orf170
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025432
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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