A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560583



Internal ID22429381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70627534..70627534hg38UCSC Ensembl
chr15:70919873..70919873hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14390289
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)nsv3560583
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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