A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17057928



Internal ID106468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:62173083..62173134hg38UCSC Ensembl
chr12:62566864..62566915hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5426436
Supporting Variants
Samples
Known GenesFAM19A2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17057928
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003278


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