A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093447



Internal ID21480107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:66798378..66798378hg38UCSC Ensembl
chr17:64794496..64794496hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38564
hg19564
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5649797
Supporting Variants
SamplesHG03683
Known GenesPRKCA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093447
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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