A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626799



Internal ID21575104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66693724..66693724hg38UCSC Ensembl
chr8:67605959..67605959hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151122
SamplesHG03065
Known GenesC8orf44-SGK3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626799
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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