A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3221882



Internal ID22366124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:47012294..47012448hg38UCSC Ensembl
chr15:47304492..47304646hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14385181
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3221882
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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