A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5695776



Internal ID21722097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11782404..11782404hg38UCSC Ensembl
chr11:11803951..11803951hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17190335
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)nsv5695776
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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