A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17121716



Internal ID21461051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27315580..27315580hg38UCSC Ensembl
chr3:27357071..27357071hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5616443
Supporting Variants
SamplesHG02818
Known GenesNEK10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17121716
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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