A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834323



Internal ID22609258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:135810563..135821309hg38UCSC Ensembl
chr3:135529405..135540151hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg3810747
hg1910747
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485105
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834323
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