A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670743



Internal ID21619048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:28414484..28420104hg38UCSC Ensembl
chr3:28455975..28461595hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg385621
hg195621
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17130395
Samples
Known GenesZCWPW2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670743
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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