A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17848706



Internal ID22032349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81435444..81435444hg38UCSC Ensembl
chr15:81727785..81727785hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38229
hg19229
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6249872
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17848706
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