A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568589



Internal ID21516938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25586393..25586508hg38UCSC Ensembl
chr6:25586621..25586736hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17139928
SamplesNA19238
Known GenesLRRC16A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568589
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