A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5677590



Internal ID21703911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35867507..35867507hg38UCSC Ensembl
chr4:35869129..35869129hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17217140, nssv17211666
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)nsv5677590
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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