A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754504



Internal ID20530364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194275714..194275714hg38UCSC Ensembl
chr3:193993503..193993503hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38941
hg19941
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276269
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754504
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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