A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702841



Internal ID126507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62661589..62661640hg38UCSC Ensembl
chr15:62953788..62953839hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5421356
Supporting Variants
Samples
Known GenesTLN2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702841
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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