A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024149



Internal ID83827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66330654..66330692hg38UCSC Ensembl
chr9:42191052..42191090hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5410813
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024149
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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