A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857374



Internal ID22632309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100213674..100221957hg38UCSC Ensembl
chr14:100680011..100688294hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg388284
hg198284
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455186
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857374
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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