A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1800n209



Internal ID22827875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131323402..131331374hg38UCSC Ensembl
chr6:131644542..131652514hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg387973
hg197973
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5844377, nsv5843753
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1800n209
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