A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5519684



Internal ID296031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65250243..65253456hg38UCSC Ensembl
chr15:65542581..65545794hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg383214
hg193214
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704256
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5519684
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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