A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17174154



Internal ID21621663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:137556845..137556845hg38UCSC Ensembl
chr4:138477999..138477999hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5675191
Supporting Variants
Samples
Known Genes
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)nssv17174154
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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