A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057746



Internal ID21966979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24813599..24813599hg38UCSC Ensembl
chr3:24855090..24855090hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547328
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057746
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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