A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17214736



Internal ID21662245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:197217322..197217322hg38UCSC Ensembl
chr2:198082046..198082046hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5674990
Supporting Variants
Samples
Known GenesANKRD44
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)nssv17214736
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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