A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17203418



Internal ID21650927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:97530052..97530052hg38UCSC Ensembl
chrX:96785051..96785051hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5730432
Supporting Variants
Samples
Known GenesDIAPH2
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)nssv17203418
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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