A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631298



Internal ID21579603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87276757..87276757hg38UCSC Ensembl
chr9:89891672..89891672hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg386076
hg196076
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162524
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631298
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