A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17684312



Internal ID107978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:108539333..108542327hg38UCSC Ensembl
chr12:108933109..108936103hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg382995
hg192995
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5510993
Supporting Variants
Samples
Known GenesSART3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17684312
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000625


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