A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5691376



Internal ID21717697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:122777249..122777249hg38UCSC Ensembl
chr4:123698404..123698404hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17211280, nssv17174604
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)nsv5691376
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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