A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767755



Internal ID20543615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:192063031..192063031hg38UCSC Ensembl
chr3:191780820..191780820hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260577
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767755
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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