A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5709805



Internal ID21736126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65756052..65756052hg38UCSC Ensembl
chr11:65523523..65523523hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17219973, nssv17191179
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)nsv5709805
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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