A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17466864



Internal ID22524755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:19919612..19920710hg38UCSC Ensembl
chrX:19937730..19938828hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg381099
hg191099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880133
Supporting Variants
Samples
Known GenesCXorf23
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17466864
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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