A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17646264



Internal ID21838311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:226048..226048hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38160
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6058391
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17646264
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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