A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025824



Internal ID84953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94917131..94917196hg38UCSC Ensembl
chr9:97679413..97679478hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480661
Supporting Variants
Samples
Known GenesC9orf3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025824
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001094


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