A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5697363



Internal ID21723684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:94898256..94898256hg38UCSC Ensembl
chr15:95441485..95441485hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17214258
Samples
Known Genes
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)nsv5697363
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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