A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17690726



Internal ID114392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:114306307..114306358hg38UCSC Ensembl
chr12:114744112..114744163hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg382813
hg192813
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562318
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17690726
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003291


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