A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5692096



Internal ID21718417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:203686428..203686428hg38UCSC Ensembl
chr2:204551151..204551151hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17210218, nssv17218621
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)nsv5692096
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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