A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5703824



Internal ID21730145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95732681..95732681hg38UCSC Ensembl
chr8:96744909..96744909hg19UCSC Ensembl
Cytoband8q22.1
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 Variantsnssv17184832, nssv17230791
Samples
Known GenesLOC100616530
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)nsv5703824
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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