A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17851498



Internal ID22035141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:21866302..21866302hg38UCSC Ensembl
chrX:21884420..21884420hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6252355
Supporting Variants
Samples
Known GenesMBTPS2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17851498
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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