A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5685552



Internal ID21711873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:17472433..17472433hg38UCSC Ensembl
chr2:17653700..17653700hg19UCSC Ensembl
Cytoband2p24.2
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 Variantsnssv17196126, nssv17205941
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)nsv5685552
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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