A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645928



Internal ID21837975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52510824..52523688hg38UCSC Ensembl
chrX:52539801..52552697hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3812865
hg1912897
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6109332
Supporting Variants
Samples
Known GenesXAGE1A, XAGE1B, XAGE1C, XAGE1D, XAGE1E
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645928
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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