A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866065



Internal ID22641000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104600450..104604711hg38UCSC Ensembl
chr14:105066787..105071048hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg384262
hg194262
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452385
Samples
Known GenesTMEM179
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866065
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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