A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17685097



Internal ID108763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122504161..122504212hg38UCSC Ensembl
chr12:122988708..122988759hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5433890
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17685097
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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