A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5696751



Internal ID21723072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98043446..98043446hg38UCSC Ensembl
chr8:99055674..99055674hg19UCSC Ensembl
Cytoband8q22.2
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 Variantsnssv17184865
Samples
Known GenesRPL30
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)nsv5696751
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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