A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835324



Internal ID22610259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:164848979..164869923hg38UCSC Ensembl
chr3:164566767..164587711hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3820945
hg1920945
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17487022
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835324
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