A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580537



Internal ID21529028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21352535..21352801hg38UCSC Ensembl
chr8:21210046..21210312hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144930
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580537
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