A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076159



Internal ID21469199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76376748..76376748hg38UCSC Ensembl
chr11:76087792..76087792hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655012
Supporting Variants
SamplesHG03125
Known GenesPRKRIR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076159
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer