A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6254076



Internal ID22058686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:59402141..59402141hg38UCSC Ensembl
chr3:59387867..59387867hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17854941
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6254076
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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