A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5688348



Internal ID21714669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:191479260..191479260hg38UCSC Ensembl
chr2:192343986..192343986hg19UCSC Ensembl
Cytoband2q32.3
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 Variantsnssv17209400, nssv17230581
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)nsv5688348
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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