A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834671



Internal ID22609606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:135574772..135612259hg38UCSC Ensembl
chr3:135293614..135331101hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg3837488
hg1937488
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485101
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834671
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