A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14399889



Internal ID22330378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:142537962..142537962hg38UCSC Ensembl
chr5:141917527..141917527hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3520631
Supporting Variants
SamplesNA19240
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)nssv14399889
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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