A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765061



Internal ID20540921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88625470..88625470hg38UCSC Ensembl
chr9:91240385..91240385hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg381194
hg191194
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267707
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765061
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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