A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14364683



Internal ID22277440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:47516042..47516042hg38UCSC Ensembl
chr12:47909825..47909825hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3559879
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
CommentsInsertion of a Alu mobile element relative to the reference
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14364683
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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