A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850670



Internal ID22625605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94192922..94200046hg38UCSC Ensembl
chr14:94659259..94666383hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg387125
hg197125
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469787
Samples
Known GenesPPP4R4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850670
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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