A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055964



Internal ID21965197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:243665174..243665174hg38UCSC Ensembl
chr1:243828476..243828476hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17528336
Samples
Known GenesAKT3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055964
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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