A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17204925



Internal ID21652434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:93946812..93946812hg38UCSC Ensembl
chrX:93201811..93201811hg19UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5721585
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)nssv17204925
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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