A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766991



Internal ID20542851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81793468..81793468hg38UCSC Ensembl
chr9:84408383..84408383hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295748
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766991
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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