A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17055613



Internal ID104908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32650612..32650793hg38UCSC Ensembl
chr12:32803546..32803727hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5503501
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17055613
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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