A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5514644



Internal ID291139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85808038..85848378hg38UCSC Ensembl
chr15:86351269..86391609hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3840341
hg1940341
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702288
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5514644
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer