A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17203861



Internal ID21651370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:25069681..25069681hg38UCSC Ensembl
chrX:25087798..25087798hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5725619
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)nssv17203861
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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