A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638677



Internal ID21586982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:117225535..117225535hg38UCSC Ensembl
chr9:119987814..119987814hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159678
SamplesHG03732
Known GenesASTN2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638677
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