A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17199246



Internal ID21646755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15330815..15330815hg38UCSC Ensembl
chr17:15234132..15234132hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5702251
Supporting Variants
Samples
Known GenesTEKT3
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)nssv17199246
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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