A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839680



Internal ID22614615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:54235870..54241720hg38UCSC Ensembl
chr4:55102037..55107887hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg385851
hg195851
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495935, nssv17495936
Samples
Known GenesPDGFRA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839680
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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