A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17178513



Internal ID21626022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150189096..150189096hg38UCSC Ensembl
chr1:150161356..150161356hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5688767
Supporting Variants
Samples
Known Genes
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a Alu mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nssv17178513
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer