A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6054641



Internal ID21963875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16684585..16684585hg38UCSC Ensembl
chr3:16726092..16726092hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17538880
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6054641
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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