A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17179035



Internal ID21626544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155740484..155740484hg38UCSC Ensembl
chr5:155120044..155120044hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5691040
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)nssv17179035
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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