A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028679



Internal ID86821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125243567..125243618hg38UCSC Ensembl
chr9:128005846..128005897hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560684
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028679
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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