A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17125626



Internal ID21508468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133885062..133885062hg38UCSC Ensembl
chr3:133603906..133603906hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5619773
Supporting Variants
SamplesNA20509
Known GenesRAB6B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17125626
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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