A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14395221



Internal ID22315657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27831211..27831211hg38UCSC Ensembl
chr2:28054078..28054078hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3520702
Supporting Variants
SamplesNA19240
Known GenesRBKS
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)nssv14395221
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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