A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17847968



Internal ID22031611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38477244..38477244hg38UCSC Ensembl
chr15:38769445..38769445hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6241946
Supporting Variants
Samples
Known GenesFAM98B
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17847968
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