A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6054891



Internal ID21964124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:245205370..245205370hg38UCSC Ensembl
chr1:245368672..245368672hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527913
Samples
Known GenesKIF26B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6054891
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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