A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626937



Internal ID21575242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89317696..89317696hg38UCSC Ensembl
chr9:91932611..91932611hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163122
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626937
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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