A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854450



Internal ID22629385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57483630..57491098hg38UCSC Ensembl
chr14:57950348..57957816hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg387469
hg197469
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452487
Samples
Known GenesC14orf105
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854450
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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