A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1987n209



Internal ID22828062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11528778..11554010hg38UCSC Ensembl
chr8:11386287..11411519hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3825233
hg1925233
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5847827, nsv5854338
Samples
Known GenesBLK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1987n209
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