A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6253996



Internal ID22058606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:50306242..50306242hg38UCSC Ensembl
chr3:50343673..50343673hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17852162
Samples
Known GenesHYAL1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6253996
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