A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5709062



Internal ID21735383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43818534..43818534hg38UCSC Ensembl
chr15:44110732..44110732hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17198057
Samples
Known GenesMFAP1
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)nsv5709062
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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