A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701009



Internal ID124675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60140472..60140817hg38UCSC Ensembl
chr15:60432671..60433016hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531339
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701009
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.004851


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