A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5630954



Internal ID21579259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98393349..98393349hg38UCSC Ensembl
chr9:101155631..101155631hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163440
SamplesNA19238
Known GenesGABBR2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5630954
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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