A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5688361



Internal ID21714682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:79478295..79478295hg38UCSC Ensembl
chr7:79107611..79107611hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17182529, nssv17225383
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)nsv5688361
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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