A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17020079



Internal ID81017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15163321..15205245hg38UCSC Ensembl
chr9:15163319..15205243hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3841925
hg1941925
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486017
Supporting Variants
Samples
Known GenesTTC39B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17020079
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001093


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