A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5682827



Internal ID21709148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7720320..7720320hg38UCSC Ensembl
chr4:7722047..7722047hg19UCSC Ensembl
Cytoband4p16.1
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 Variantsnssv17222310
Samples
Known GenesSORCS2
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)nsv5682827
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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