A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17218405



Internal ID21665914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23031187..23031187hg38UCSC Ensembl
chr10:23320116..23320116hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5704498
Supporting Variants
Samples
Known GenesARMC3
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)nssv17218405
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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