A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027500



Internal ID86040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95830552..95837200hg38UCSC Ensembl
chr9:98592834..98599482hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg386649
hg196649
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5481296
Supporting Variants
Samples
Known GenesLINC00476
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027500
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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