A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17236779



Internal ID21684288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14626146..14626146hg38UCSC Ensembl
chr11:14647692..14647692hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg386017
hg196017
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5728485
Supporting Variants
Samples
Known GenesPSMA1
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a L1 mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nssv17236779
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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