A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6247177



Internal ID22051787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:66157078..66157078hg38UCSC Ensembl
chr10:67916836..67916836hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17841955
Samples
Known GenesCTNNA3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6247177
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