A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17223525



Internal ID21671034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:100667725..100667725hg38UCSC Ensembl
chrX:99922722..99922722hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5718175
Supporting Variants
Samples
Known GenesSRPX2
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)nssv17223525
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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