A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766026



Internal ID20541886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87402455..87402455hg38UCSC Ensembl
chr9:90017370..90017370hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291004
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766026
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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