A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17105353



Internal ID21449096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3961353..3961353hg38UCSC Ensembl
chr19:3961351..3961351hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5645574
Supporting Variants
SamplesHG00864
Known GenesDAPK3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17105353
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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