A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864336



Internal ID22639271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:54414059..54417708hg38UCSC Ensembl
chr14:54880777..54884426hg19UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg383650
hg193650
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466476
Samples
Known GenesCDKN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864336
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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