A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5682522



Internal ID21708843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41190165..41190165hg38UCSC Ensembl
chr6:41157903..41157903hg19UCSC Ensembl
Cytoband6p21.1
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 Variantsnssv17179567
Samples
Known GenesTREML2
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)nsv5682522
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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