A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867104



Internal ID22642039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110518163..110523702hg38UCSC Ensembl
chr9:113280443..113285982hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg385540
hg195540
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2180n209
Supporting Variantsnssv17510744
Samples
Known GenesSVEP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867104
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