A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5693128



Internal ID21719449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:75489671..75489671hg38UCSC Ensembl
chr2:75716797..75716797hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17209000, nssv17204848
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)nsv5693128
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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