A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5696033



Internal ID21722354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50984624..50984624hg38UCSC Ensembl
chr12:51378407..51378407hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17190940
Samples
Known GenesSLC11A2
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)nsv5696033
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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