A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14448238



Internal ID22223071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35689269..35689269hg38UCSC Ensembl
chr19:36180171..36180171hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3524482
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)nssv14448238
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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