A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025826



Internal ID84954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94928928..94930776hg38UCSC Ensembl
chr9:97691210..97693058hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg381849
hg191849
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485229
Supporting Variants
Samples
Known GenesC9orf3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025826
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer