A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704163



Internal ID127829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89989575..89993069hg38UCSC Ensembl
chr15:90532807..90536301hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg383495
hg193495
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519423
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704163
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003283


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