A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6254755



Internal ID22059365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141382297..141382297hg38UCSC Ensembl
chr3:141101139..141101139hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17852753
Samples
Known GenesZBTB38
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6254755
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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