A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17231696



Internal ID21679205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119330355..119330355hg38UCSC Ensembl
chr10:121089867..121089867hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5702972
Supporting Variants
Samples
Known GenesGRK5
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)nssv17231696
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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