A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842044



Internal ID22025687
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 StatusS
Merged Variantsnsv6240468
Supporting Variants
Samples
Known GenesC10orf115
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842044
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