A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17219973



Internal ID21667482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65756052..65756052hg38UCSC Ensembl
chr11:65523523..65523523hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5709805
Supporting Variants
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)nssv17219973
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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