A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764093



Internal ID20539953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184712979..184712979hg38UCSC Ensembl
chr3:184430767..184430767hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260038
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764093
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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