A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5696912



Internal ID21723233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:115599599..115599599hg38UCSC Ensembl
chr12:116037404..116037404hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17193969
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)nsv5696912
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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