A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109332



Internal ID22018565
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 StatusM
Merged Variants
Supporting Variantsnssv17645928
Samples
Known GenesXAGE1A, XAGE1B, XAGE1C, XAGE1D, XAGE1E
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109332
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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