A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17202290



Internal ID21649799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:26397668..26397668hg38UCSC Ensembl
chrX:26415785..26415785hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5724561
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)nssv17202290
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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