A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835015



Internal ID22609950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158766012..158792344hg38UCSC Ensembl
chr3:158483801..158510133hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3826333
hg1926333
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486491
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835015
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