A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17844062



Internal ID22027705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25960476..25960476hg38UCSC Ensembl
chr12:26113409..26113409hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6240807
Supporting Variants
Samples
Known GenesRASSF8
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17844062
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