A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760497



Internal ID20536357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47264999..47264999hg38UCSC Ensembl
chr3:47306489..47306489hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294594
Samples
Known GenesKIF9
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760497
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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