A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835094



Internal ID22610029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16611315..16617264hg38UCSC Ensembl
chr3:16652822..16658771hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg385950
hg195950
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17487070
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835094
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