A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766578



Internal ID20542438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128152892..128152892hg38UCSC Ensembl
chr3:127871735..127871735hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293794
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766578
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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