A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17198277



Internal ID21645786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3112516..3112516hg38UCSC Ensembl
chr16:3162517..3162517hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5694428
Supporting Variants
Samples
Known GenesZNF205-AS1
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)nssv17198277
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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