A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701879



Internal ID125545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:32821096..32821096hg38UCSC Ensembl
chr15:33113297..33113297hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422893
Supporting Variants
Samples
Known GenesFMN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701879
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.192038


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