A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635671



Internal ID21583976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108900775..108900775hg38UCSC Ensembl
chr9:111663055..111663055hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158443
SamplesHG03486
Known GenesIKBKAP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635671
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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