A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17179493



Internal ID21627002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25085467..25085467hg38UCSC Ensembl
chr6:25085695..25085695hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5688644
Supporting Variants
Samples
Known GenesCMAHP
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)nssv17179493
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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