A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17849324



Internal ID22032967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:41526799..41526799hg38UCSC Ensembl
chr18:39106763..39106763hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6242339
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17849324
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