A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6240468



Internal ID22045078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23215769..23215769hg38UCSC Ensembl
chr10:23504698..23504698hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17842044
Samples
Known GenesC10orf115
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6240468
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