A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5688718



Internal ID21715039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:144721612..144721612hg38UCSC Ensembl
chr4:145642764..145642764hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17174711
Samples
Known GenesHHIP
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)nsv5688718
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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