A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837843



Internal ID22612778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:114810170..114813666hg38UCSC Ensembl
chr4:115731326..115734822hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg383497
hg193497
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17498234
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837843
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