A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515222



Internal ID291706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88483054..88501316hg38UCSC Ensembl
chr15:89026285..89044547hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3818263
hg1918263
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17705520
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515222
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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