A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836170



Internal ID22611105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33486651..33497429hg38UCSC Ensembl
chr3:33528143..33538921hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3810779
hg1910779
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490682
Samples
Known GenesCLASP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836170
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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