A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5694713



Internal ID21721034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44903486..44903486hg38UCSC Ensembl
chr22:45299366..45299366hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17203805, nssv17225940
Samples
Known GenesPHF21B
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)nsv5694713
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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