A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5684376



Internal ID21710697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:100909700..100909700hg38UCSC Ensembl
chr1:101375256..101375256hg19UCSC Ensembl
Cytoband1p21.2
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 Variantsnssv17175496
Samples
Known GenesSLC30A7
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a Alu mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nsv5684376
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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