A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532186



Internal ID308114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98194427..98194494hg38UCSC Ensembl
chr15:98737656..98737723hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17705201
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532186
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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