A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561672



Internal ID22430440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56413390..56413390hg38UCSC Ensembl
chr1:56879062..56879062hg19UCSC Ensembl
Cytoband1p32.2
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 Variantsnssv14368134
SamplesHG00731
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)nsv3561672
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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