A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590353



Internal ID21538922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92771249..92772757hg38UCSC Ensembl
chr15:93314479..93315987hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381509
hg191509
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081577
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590353
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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