A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641270



Internal ID21589575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111642015..111642015hg38UCSC Ensembl
chr9:114404295..114404295hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38409
hg19409
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159621
SamplesNA19238
Known GenesDNAJC25, DNAJC25-GNG10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641270
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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