A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17361860



Internal ID22587529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:66019711..66633925hg38UCSC Ensembl
chr10:67779469..68393683hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38614215
hg19614215
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5921449
Supporting Variants
Samples
Known GenesCTNNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17361860
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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