A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv76n209



Internal ID22826151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:124266891..124594055hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38327165
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5878449, nsv5885293
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv76n209
Frequency
Sample Size914
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer