A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17017774



Internal ID79498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:1113774..1221775hg38UCSC Ensembl
chr9:1113774..1221775hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38108002
hg19108002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5481998
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17017774
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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