A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5702736



Internal ID21729057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:25140856..25140856hg38UCSC Ensembl
chr11:25162402..25162402hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17216662, nssv17188955
Samples
Known Genes
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)nsv5702736
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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