A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17717118



Internal ID140784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:32067048..32098621hg38UCSC Ensembl
chr18:29647011..29678584hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3831574
hg1931574
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521276
Supporting Variants
Samples
Known GenesRNF125, RNF138
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17717118
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001874


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