A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17203976



Internal ID21651485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:15842242..15842242hg38UCSC Ensembl
chr21:17214561..17214561hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5702877
Supporting Variants
Samples
Known GenesUSP25
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)nssv17203976
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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