A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759270



Internal ID20535130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42506892..42506892hg38UCSC Ensembl
chr3:42548384..42548384hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280060
Samples
Known GenesVIPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759270
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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