A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17204516



Internal ID21652025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:35637861..35637861hg38UCSC Ensembl
chrX:35655978..35655978hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5721888
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)nssv17204516
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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