A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763380



Internal ID20539240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32420101..32420101hg38UCSC Ensembl
chr9:32420099..32420099hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289252
Samples
Known GenesACO1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763380
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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