A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17184978



Internal ID21632487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92813097..92813097hg38UCSC Ensembl
chr8:93825325..93825325hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5711480
Supporting Variants
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)nssv17184978
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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