A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17416492



Internal ID22474362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:34893461..34893461hg38UCSC Ensembl
chr3:34934953..34934953hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38408
hg19408
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5963721
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17416492
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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