A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17234755



Internal ID21682264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119842326..119842326hg38UCSC Ensembl
chr3:119561173..119561173hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg382127
hg192127
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5714350
Supporting Variants
Samples
Known GenesGSK3B
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)nssv17234755
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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