A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5691106



Internal ID21717427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:72576271..72576271hg38UCSC Ensembl
chr5:71872098..71872098hg19UCSC Ensembl
Cytoband5q13.2
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 Variantsnssv17176279
Samples
Known GenesLOC102477328
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)nsv5691106
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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