A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5697741



Internal ID21724062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100637968..100637968hg38UCSC Ensembl
chr15:101178173..101178173hg19UCSC Ensembl
Cytoband15q26.3
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 Variantsnssv17197176, nssv17219352
Samples
Known GenesASB7
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)nsv5697741
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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