A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3564426



Internal ID22433156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160915415..160915415hg38UCSC Ensembl
chr6:161336447..161336447hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14330593, nssv14330594
SamplesHG00731, HG00733
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)nsv3564426
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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