A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094055



Internal ID21401602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23301429..23301429hg38UCSC Ensembl
chr14:23770638..23770638hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5646739
Supporting Variants
SamplesHG00096
Known GenesPPP1R3E
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094055
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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