A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3563872



Internal ID22432608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161739399..161739399hg38UCSC Ensembl
chr5:161166405..161166405hg19UCSC Ensembl
Cytoband5q34
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 Variantsnssv14325204, nssv14325205
SamplesHG00512, HG00514
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)nsv3563872
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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