A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17850838



Internal ID22034481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:4366544..4366544hg38UCSC Ensembl
chrX:4284585..4284585hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6252262
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17850838
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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