A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028095



Internal ID86426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129519004..129520620hg38UCSC Ensembl
chr9:132281283..132282899hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381617
hg191617
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484096
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028095
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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