A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5553518



Internal ID326757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104290178..104290178hg38UCSC Ensembl
chr12:104683956..104683956hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17690514
Samples
Known GenesTXNRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5553518
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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