A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732284



Internal ID155950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37856610..37856661hg38UCSC Ensembl
chr20:36485012..36485063hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5417801
Supporting Variants
Samples
Known GenesCTNNBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732284
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.005151


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