A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17520230



Internal ID21844589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:214622754..214622754hg38UCSC Ensembl
chr1:214796097..214796097hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6046674
Supporting Variants
Samples
Known GenesCENPF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17520230
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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