A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636265



Internal ID21584570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94147773..94147773hg38UCSC Ensembl
chr9:96910055..96910055hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163745
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636265
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