A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2104n209



Internal ID22828179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39470728..39478755hg38UCSC Ensembl
chr9:41615746..41623773hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg388028
hg198028
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5852527, nsv5865843
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv2104n209
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