A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5632119



Internal ID21580424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66720613..66720613hg38UCSC Ensembl
chr8:67632848..67632848hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157485
SamplesHG03125
Known GenesC8orf44-SGK3, SGK3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5632119
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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