A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035576



Internal ID91465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:66019711..66633929hg38UCSC Ensembl
chr10:67779469..68393687hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38614219
hg19614219
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483767
Supporting Variants
Samples
Known GenesCTNNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035576
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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