A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702893



Internal ID126559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64065236..64066630hg38UCSC Ensembl
chr15:64357435..64358829hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381395
hg191395
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531547
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702893
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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