A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5708690



Internal ID21735011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:112249738..112249738hg38UCSC Ensembl
chr12:112687542..112687542hg19UCSC Ensembl
Cytoband12q24.13
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 Variantsnssv17193366
Samples
Known GenesHECTD4
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)nsv5708690
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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