A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027483



Internal ID86030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95658598..95658635hg38UCSC Ensembl
chr9:98420880..98420917hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5553657
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027483
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.009522


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