A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5709036



Internal ID21735357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21099011..21099011hg38UCSC Ensembl
chr14:21567170..21567170hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17194671, nssv17214696
Samples
Known GenesTMEM253, ZNF219
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)nsv5709036
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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