A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834340



Internal ID22609275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141654556..141674227hg38UCSC Ensembl
chr3:141373398..141393069hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3819672
hg1919672
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485187
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834340
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