A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17700912



Internal ID124578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58769285..58769562hg38UCSC Ensembl
chr15:59061484..59061761hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5532792
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17700912
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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