A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17232175



Internal ID21679684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:109818606..109818606hg38UCSC Ensembl
chrX:109061835..109061835hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5717943
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)nssv17232175
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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