A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17208727



Internal ID21656236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:215412782..215412782hg38UCSC Ensembl
chr2:216277505..216277505hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5677092
Supporting Variants
Samples
Known GenesFN1
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)nssv17208727
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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