A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027813



Internal ID86240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:115162016..115162052hg38UCSC Ensembl
chr9:117924295..117924331hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5546807
Supporting Variants
Samples
Known GenesDEC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027813
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.069869


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