A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17690498



Internal ID114164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104052902..104055223hg38UCSC Ensembl
chr12:104446680..104449001hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg382322
hg192322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5495955
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17690498
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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