A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14451554



Internal ID22219728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:51729913..51729913hg38UCSC Ensembl
chr3:51763929..51763929hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3524010
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsInsertion of a AluY mobile element relative to the reference
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14451554
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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