A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5702196



Internal ID21728517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1472806..1472806hg38UCSC Ensembl
chr17:1376100..1376100hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17198852, nssv17232305
Samples
Known GenesMYO1C
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)nsv5702196
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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