A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6253720



Internal ID22058330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13911882..13911882hg38UCSC Ensembl
chr3:13953379..13953379hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17852093
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6253720
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer