A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766873



Internal ID20542733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91132622..91132622hg38UCSC Ensembl
chr9:93894904..93894904hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278189
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766873
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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