A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857850



Internal ID22632785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60523056..60527284hg38UCSC Ensembl
chr14:60989774..60994002hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg384229
hg194229
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453760, nssv17465225
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857850
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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