A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17685775



Internal ID109441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:133101132..133186349hg38UCSC Ensembl
chr12:133677718..133762935hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3885218
hg1985218
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5499188
Supporting Variants
Samples
Known GenesZNF10, ZNF140, ZNF268, ZNF891
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17685775
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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