A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645880



Internal ID21837927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:17518032..17518032hg38UCSC Ensembl
chr21:18890350..18890350hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6105568
Supporting Variants
Samples
Known GenesCXADR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645880
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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