A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533189



Internal ID309087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44735269..44735412hg38UCSC Ensembl
chr15:45027467..45027610hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701622
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533189
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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