A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046674



Internal ID21955907
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 StatusM
Merged Variants
Supporting Variantsnssv17520230
Samples
Known GenesCENPF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046674
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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