A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5994168



Internal ID21903511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:76534029..76538143hg38UCSC Ensembl
chr3:76583180..76587294hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg384115
hg194115
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550004
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5994168
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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