A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17684168



Internal ID107834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93945686..93945686hg38UCSC Ensembl
chr12:94339462..94339462hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38791
hg19791
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5553328
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17684168
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.017636


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