A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17096062



Internal ID21508636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68352089..68352089hg38UCSC Ensembl
chr16:68385992..68385992hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653164
Supporting Variants
SamplesNA20509
Known GenesPRMT7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17096062
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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