A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835509



Internal ID22610444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194171052..194174754hg38UCSC Ensembl
chr3:193888841..193892543hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg383703
hg193703
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490417
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835509
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