A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17202123



Internal ID21649632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:29110280..29110280hg38UCSC Ensembl
chr22:29506268..29506268hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5710906
Supporting Variants
Samples
Known GenesKREMEN1
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)nssv17202123
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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