A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765817



Internal ID20541677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:102504036..102504036hg38UCSC Ensembl
chr9:105266318..105266318hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259545
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765817
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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