A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046362



Internal ID21955606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15272604..15272604hg38UCSC Ensembl
chr3:15314111..15314111hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552649
Samples
Known GenesSH3BP5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046362
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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