A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070003



Internal ID21979236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66803433..66803433hg38UCSC Ensembl
chr8:67715668..67715668hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584648
Samples
Known GenesC8orf44-SGK3, SGK3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070003
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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