A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17200912



Internal ID21648421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36012491..36012491hg38UCSC Ensembl
chr1:36478092..36478092hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5692885
Supporting Variants
Samples
Known GenesAGO3
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)nssv17200912
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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