A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17085758



Internal ID21445454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80663084..80663084hg38UCSC Ensembl
chr16:80696981..80696981hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5664504
Supporting Variants
SamplesHG00732
Known GenesCDYL2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17085758
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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