A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5675578



Internal ID21701899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4526893..4526893hg38UCSC Ensembl
chr4:4528620..4528620hg19UCSC Ensembl
Cytoband4p16.2
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 Variantsnssv17229703
Samples
Known GenesSTX18
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)nsv5675578
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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