A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14382977



Internal ID22288720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25112545..25112545hg38UCSC Ensembl
chr14:25581751..25581751hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3521726
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)nssv14382977
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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